- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT00153101
Effektivitet og sikkerhed af ramipril alene sammenlignet med telmisartan alene og i kombination med ramipril hos patienter med høj risiko for kardiovaskulære hændelser. Patienter, der var intolerante over for Ramipril, blev optaget i TRANSCEND, Telmisartan sammenlignet med placebo.
ONTARGET Igangværende Telmisartan alene og i kombination med Ramipril Global Endpoint Trial Et stort, simpelt randomiseret forsøg med en angiotensin II-receptorantagonist (Telmisartan) og en ACE-hæmmer (Ramipril) hos patienter med høj risiko for kardiovaskulære hændelser og TRANSCENDT tilfældig undersøgelse i Telmisartan aCE intolerante forsøgspersoner med hjerte-kar-sygdomme. En parallel undersøgelse, der sammenligner virkningerne af telmisartan med placebo og resultater hos patienter med høj risiko for kardiovaskulære hændelser og intolerante over for ACE-I.
Den igangværende telmisartan alene og i kombination med Ramipril Global Endpoint-studie (ONTARGET): De primære mål er at bestemme, om (a) telmisartan 80 mg daglig og ramipril 10 mg daglig kombinationsbehandling er mere effektiv til at reducere det sammensatte endepunkt af kardiovaskulær død (CV) død , Myokardieinfarkt (MI), slagtilfælde eller hospitalsindlæggelse for kongestiv hjertesvigt (CHF) sammenlignet med ramipril 10 mg alene; og (b) telmisartan 80 mg dagligt er mindst lige så effektivt som (dvs. ikke mindre effektiv end) ramipril 10 mg dagligt på dette endepunkt.
Telmisartan Randomized Assessment Study i angiotensionskonverterende enzymhæmmer intolerante forsøgspersoner med kardiovaskulær sygdom. (TRANSCEND): Det primære formål med undersøgelsen er at bestemme, om behandling med telmisartan 80 mg dagligt er bedre end placebo, hvilket reducerer det sammensatte endepunkt af kardiovaskulær død (CV), myokardieinfarkt (MI)I, slagtilfælde eller hospitalsindlæggelse for kongestiv hjertesvigt (CHF). ) hos patienter, der er intolerante over for angiotensionskonverterende enzymhæmmere.
Studieoversigt
Status
Betingelser
Intervention / Behandling
Undersøgelsestype
Tilmelding (Faktiske)
Fase
- Fase 4
Kontakter og lokationer
Studiesteder
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Capital Federal, Argentina
- 502.373.350 Boehringer Ingelheim Investigational Site
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Capital Federal, Argentina
- 502.373.351 Boehringer Ingelheim Investigational Site
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Capital Federal, Argentina
- 502.373.352 Boehringer Ingelheim Investigational Site
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Capital Federal, Argentina
- 502.373.353 Boehringer Ingelheim Investigational Site
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Capital Federal, Argentina
- 502.373.354 Boehringer Ingelheim Investigational Site
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Capital Federal, Argentina
- 502.373.355 Boehringer Ingelheim Investigational Site
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Capital Federal, Argentina
- 502.373.356 Boehringer Ingelheim Investigational Site
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Capital Federal, Argentina
- 502.373.378 Boehringer Ingelheim Investigational Site
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Corones Suárez, Argentina
- 502.373.362 Boehringer Ingelheim Investigational Site
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Córdoba, Argentina
- 502.373.357 Boehringer Ingelheim Investigational Site
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Córdoba, Argentina
- 502.373.358 Boehringer Ingelheim Investigational Site
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Córdoba, Argentina
- 502.373.360 Boehringer Ingelheim Investigational Site
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Córdoba, Argentina
- 502.373.361 Boehringer Ingelheim Investigational Site
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Córdoba, Argentina
- 502.373.377 Boehringer Ingelheim Investigational Site
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La Plata, Argentina
- 502.373.364 Boehringer Ingelheim Investigational Site
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Mar del Plata, Argentina
- 502.373.365 Boehringer Ingelheim Investigational Site
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Mendoza, Argentina
- 502.373.366 Boehringer Ingelheim Investigational Site
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Mendoza, Argentina
- 502.373.376 Boehringer Ingelheim Investigational Site
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Rosario, Argentina
- 502.373.367 Boehringer Ingelheim Investigational Site
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Salta, Argentina
- 502.373.369 Boehringer Ingelheim Investigational Site
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Santa Fe, Argentina
- 502.373.375 Boehringer Ingelheim Investigational Site
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Tucumán, Argentina
- 502.373.371 Boehringer Ingelheim Investigational Site
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Tucumán, Argentina
- 502.373.373 Boehringer Ingelheim Investigational Site
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Zárate, Argentina
- 502.373.374 Boehringer Ingelheim Investigational Site
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Australian Capital Territory
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Woden, Australian Capital Territory, Australien
- 502.373.0534 The Canberra Hospital
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New South Wales
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Camperdown, New South Wales, Australien
- 502.373.0536 Royal Prince Alfred Hospital
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Coffs Harbour, New South Wales, Australien
- 502.373.0544 Coffs Harbour Cardiovascular Clinic
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Concord, New South Wales, Australien
- 502.373.0538 Concord Repatriation General Hospital
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Gosford, New South Wales, Australien
- 502.373.0539 Central Coast Neuroscience Research
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Gosford, New South Wales, Australien
- 502.373.0556 Gosford Hospital
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Kogarah, New South Wales, Australien
- 502.373.0542 St. George Hospital
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Kogarah, New South Wales, Australien
- 502.373.0552 St George Private Hospital
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Kogarah, New South Wales, Australien
- 502.373.0559 St George Hospital - Dept of Clinical Pharmacology
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Newcastle, New South Wales, Australien
- 502.373.0528 John Hunter Hospital
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Randwick, New South Wales, Australien
- 502.373.0535 The Prince of Wales Hospital
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St Leonards, New South Wales, Australien
- 502.373.0533 Royal North Shore Hospital
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Wollongong, New South Wales, Australien
- 502.373.0549 Illawarra Regional Hospital
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Queensland
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Chermside, Queensland, Australien
- 502.373.0523 The Prince Charles Hospital
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Herston, Queensland, Australien
- 502.373.0524 Royal Brisbane Hospital
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Kippa-Ring, Queensland, Australien
- 502.373.0526 Peninsula Clinical Research Centre
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Southport, Queensland, Australien
- 502.373.0540 Gold Coast Hospital
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Woolloongabba, Queensland, Australien
- 502.373.0521 Princess Alexandra Hospital
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South Australia
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Bedford Park, South Australia, Australien
- 502.373.0546 Flinders Medical Centre
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Daw Park, South Australia, Australien
- 502.373.0550 Repatriation General Hospital
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Port Lincoln, South Australia, Australien
- 502.373.0551 Port Lincoln "The Investigator" Clinic
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Tasmania
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Launceston, Tasmania, Australien
- 502.373.0529 Launceston General Hospital
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Victoria
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Box Hill, Victoria, Australien
- 502.373.0531 Box Hill Hospital
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Epping, Victoria, Australien
- 502.373.0548 The Northern Hospital
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Geelong, Victoria, Australien
- 502.373.0522 The Geelong Hospital
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Parkville, Victoria, Australien
- 502.373.0520 Royal Melbourne Hospital
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Prahran, Victoria, Australien
- 502.373.0525 The Alfred Hospital
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Prahran, Victoria, Australien
- 502.373.0532 Baker Medical Research Centre
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Ringwood East, Victoria, Australien
- 502.373.0557 Maroondah Hospital
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West Heidelberg, Victoria, Australien
- 502.373.0537 Austin & Repatriation Medical Centre
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Western Australia
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Fremantle, Western Australia, Australien
- 502.373.0547 Fremantle Hospital
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Nedlands, Western Australia, Australien
- 502.373.0530 Sir Charles Gairdner Hospital
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Perth, Western Australia, Australien
- 502.373.0545 Royal Perth Hospital
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Aalst, Belgien
- 502.373.1004 Boehringer Ingelheim Investigational Site
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Anderlecht, Belgien
- 502.373.1015 Boehringer Ingelheim Investigational Site
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Antwerpen, Belgien
- 502.373.1005 Boehringer Ingelheim Investigational Site
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Bornem, Belgien
- 502.373.1022 Boehringer Ingelheim Investigational Site
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Brasschaat, Belgien
- 502.373.1021 Boehringer Ingelheim Investigational Site
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Brugge, Belgien
- 502.373.1003 Boehringer Ingelheim Investigational Site
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Charleroi, Belgien
- 502.373.1017 Boehringer Ingelheim Investigational Site
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Genk, Belgien
- 502.373.1009 Boehringer Ingelheim Investigational Site
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Godinne, Belgien
- 502.373.1018 Boehringer Ingelheim Investigational Site
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Haine-Saint-Paul, Belgien
- 502.373.1011 Boehringer Ingelheim Investigational Site
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Haine-Saint-Paul, Belgien
- 502.373.1019 Boehringer Ingelheim Investigational Site
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Hasselt, Belgien
- 502.373.1007 Boehringer Ingelheim Investigational Site
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Leuven, Belgien
- 502.373.1000 Boehringer Ingelheim Investigational Site
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Mechelen, Belgien
- 502.373.1020 Boehringer Ingelheim Investigational Site
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Mol, Belgien
- 502.373.1006 Boehringer Ingelheim Investigational Site
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Roeselare, Belgien
- 502.373.1028 Boehringer Ingelheim Investigational Site
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Seraing, Belgien
- 502.373.1014 Boehringer Ingelheim Investigational Site
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Turnhout, Belgien
- 502.373.1002 Boehringer Ingelheim Investigational Site
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Turnhout, Belgien
- 502.373.1010 Boehringer Ingelheim Investigational Site
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Woluwé-Saint-Lambert, Belgien
- 502.373.1025 Boehringer Ingelheim Investigational Site
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Belo Horizonte, Brasilien
- 502.373.405 Boehringer Ingelheim Investigational Site
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Belo Horizonte, Brasilien
- 502.373.412 Boehringer Ingelheim Investigational Site
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Belo Horizonte, Brasilien
- 502.373.426 Boehringer Ingelheim Investigational Site
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Botucatu -, Brasilien
- 502.373.418 Boehringer Ingelheim Investigational Site
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Campinas, Brasilien
- 502.373.407 Boehringer Ingelheim Investigational Site
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Campinas, Brasilien
- 502.373.419 Boehringer Ingelheim Investigational Site
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Cerqueira César - São Paulo, Brasilien
- 502.373.425 Boehringer Ingelheim Investigational Site
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Curitiba, Brasilien
- 502.373.406 Boehringer Ingelheim Investigational Site
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Goiania, Brasilien
- 502.373.411 Boehringer Ingelheim Investigational Site
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Marília, Brasilien
- 502.373.403 Boehringer Ingelheim Investigational Site
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Pelotas, Brasilien
- 502.373.400 Boehringer Ingelheim Investigational Site
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Porto Alegre, Brasilien
- 502.373.416 Boehringer Ingelheim Investigational Site
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Porto Alegre, Brasilien
- 502.373.417 Boehringer Ingelheim Investigational Site
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Porto Alegre - Rs, Brasilien
- 502.373.415 Boehringer Ingelheim Investigational Site
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Ribeirao Preto, Brasilien
- 502.373.420 Boehringer Ingelheim Investigational Site
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Rio de Janeiro, Brasilien
- 502.373.414 Boehringer Ingelheim Investigational Site
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Rio de Janeiro - Rj, Brasilien
- 502.373.413 Boehringer Ingelheim Investigational Site
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Salvador, Brasilien
- 502.373.409 Boehringer Ingelheim Investigational Site
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Salvador, Brasilien
- 502.373.410 Boehringer Ingelheim Investigational Site
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Santa Catalina, Brasilien
- 502.373.404 Boehringer Ingelheim Investigational Site
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Sao Jose do Rio Preto, Brasilien
- 502.373.421 Boehringer Ingelheim Investigational Site
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Sao Paulo, Brasilien
- 502.373.422 Boehringer Ingelheim Investigational Site
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São Paulo, Brasilien
- 502.373.402 Boehringer Ingelheim Investigational Site
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São Paulo, Brasilien
- 502.373.408 Boehringer Ingelheim Investigational Site
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São Paulo, Brasilien
- 502.373.424 Boehringer Ingelheim Investigational Site
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Vila Clementino, São Paulo, Brasilien
- 502.373.423 Boehringer Ingelheim Investigational Site
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Manitoba, Canada
- 502.373.0030 Portage Clinical Studies
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Quebec, Canada
- 502.373.0028 Hop. Du St. Sacrement
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Quebec, Canada
- 502.373.0041 Recherches Clinicar Inc.
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Quebec, Canada
- 502.373.0080 Polyclinique vasculaire Centre hospitalier universitaire de
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Quebec, Canada
- 502.373.0084 CHA-Hopital de l'Efant-Jesus
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Alberta
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Calgary, Alberta, Canada
- 502.373.0001 C849 Division of Cardiology, Foothills Medical Centre
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Calgary, Alberta, Canada
- 502.373.0071 Peter Lougheed Centre
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Edmonton, Alberta, Canada
- 502.373.0020 CHA/University Hospital
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British Columbia
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Campbell river, British Columbia, Canada
- 502.373.0073 Alder Medical Centre
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Coquitlam, British Columbia, Canada
- 502.373.0062 Gain Medical Centre
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Kelowna, British Columbia, Canada
- 502.373.0046 Interior Clinical Research Consultants Ltd
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New Westminster, British Columbia, Canada
- 502.373.0038 New West Cardiac Research
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North Vancouver, British Columbia, Canada
- 502.373.0048 Suite 100
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Penticton, British Columbia, Canada
- 502.373.0002 Penticton Regional Hospital
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Vancouver, British Columbia, Canada
- 502.373.0009 Vancouver Hospital
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Victoria, British Columbia, Canada
- 502.373.0003 Discovery Clinical Services Ltd
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Manitoba
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St. Pierre, Manitoba, Canada
- 502.373.0050 St. Pierre Medical Clinic
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Winnipeg, Manitoba, Canada
- 502.373.0077 Health Science Centre Diabetes Research Group
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Newfoundland and Labrador
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ST John's, Newfoundland and Labrador, Canada
- 502.373.0005 Dr. Jeffrey Hiscock
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St. John's, Newfoundland and Labrador, Canada
- 502.373.0006 The General Hospital
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Nova Scotia
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Antigonish, Nova Scotia, Canada
- 502.373.0056 Antigonish Clinical Trials
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Halifax, Nova Scotia, Canada
- 502.373.0045 Queen Elizabeth II HSC
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Ontario
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Brampton, Ontario, Canada
- 502.373.0031 Brampton Research Associates
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Hamilton, Ontario, Canada
- 502.373.0011 St. Joseph's Hospital Cardiac Research
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Hamilton, Ontario, Canada
- 502.373.0034 HGH McMaster Clinic
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Hamilton, Ontario, Canada
- 502.373.0035 Hamilton Medical Research
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Hamilton, Ontario, Canada
- 502.373.0064 Chedoke Hospital
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Hamilton, Ontario, Canada
- 502.373.0082 3U4, McMaster University Medical Centre
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Hamilton, Ontario, Canada
- 502.373.0085 HGH McMaster Clinic
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London, Ontario, Canada
- 502.373.0024 London HSC - University Hospital
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Mississauga, Ontario, Canada
- 502.373.0044 Mississauga Clinical Research Centre
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New Westminster, Ontario, Canada
- 502.373.0043 Fraser Clinical Trial Inc
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Newmarket, Ontario, Canada
- 502.373.0032 New Market Cardiology Research Grp
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Niagara Falls, Ontario, Canada
- 502.373.0037 Niagara Falls Medical Centre
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Orleans, Ontario, Canada
- 502.373.0054 Orleans Medical-Dental Centre
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Oshawa, Ontario, Canada
- 502.373.0058 Medical Sciences Building
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Oshawa, Ontario, Canada
- 502.373.0063 Paradigm Clinical Trials
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Ottawa, Ontario, Canada
- 502.373.0029 Riverside Professional Building
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Ottawa, Ontario, Canada
- 502.373.0051 Merivale Cardiovascular Consultants
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Rexdale, Ontario, Canada
- 502.373.0040 Etobicok Cardiology
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Sault Ste Marie, Ontario, Canada
- 502.373.0023 Group Health Centre - Clinical Trials
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Scarborough, Ontario, Canada
- 502.373.0039 Scarborough Cardiology Research
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Sudbury, Ontario, Canada
- 502.373.0007 Sudbury Cardiac Research
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Thunder Bay, Ontario, Canada
- 502.373.0061 CLIKS Medical Research Corp
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Toronto, Ontario, Canada
- 502.373.0042 Sunnybrook & Woman's College Health Science Centre
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Toronto, Ontario, Canada
- 502.373.0083 St. Michael's Hospital
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Willowdale, Ontario, Canada
- 502.373.0052 Dr. Bruce Lubelsky
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Windsor, Ontario, Canada
- 502.373.0008 Windsor Health Clinic
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Quebec
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Fleurimont, Quebec, Canada
- 502.373.0081 Centre de recherche clinique, CUSE 3001
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Gatineau, Quebec, Canada
- 502.373.0076 Centre Hospitalier de Vallees de l'Outaouais Gatineau
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Laval, Quebec, Canada
- 502.373.0057 Centre De Recherche Clinique
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Levis, Quebec, Canada
- 502.373.0033 Clinique de Cardiologie de Levis
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Longueuil, Quebec, Canada
- 502.373.0010 Recherche Invascor
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Longueuil, Quebec, Canada
- 502.373.0013 Suite 170
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Longueuil, Quebec, Canada
- 502.373.0014 Via Car Recherche Clinique Inc
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Longueuil, Quebec, Canada
- 502.373.0015 C/O Peter Carmichael
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Longueuil, Quebec, Canada
- 502.373.0016 Suite 170
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Longueuil, Quebec, Canada
- 502.373.0017 Suite 170
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Longueuil, Quebec, Canada
- 502.373.0086 Via Car Recherche Clinique Inc
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Montreal, Quebec, Canada
- 502.373.0018 Montreal Heart Institute
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Montreal, Quebec, Canada
- 502.373.0021 Medi - recherche Inc.
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Montreal, Quebec, Canada
- 502.373.0022 CHUM - Hotel Dieu
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Montreal, Quebec, Canada
- 502.373.0025 Hopital Maisonneuve Rosemont
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Montreal, Quebec, Canada
- 502.373.0079 Jewish General Hospital
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St George de Beauce, Quebec, Canada
- 502.373.0027 Ctr Hospitalier Beauce Etchemin
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Ste-Foy, Quebec, Canada
- 502.373.0012 Hopital Laval - Institute Cardiologie de Quebec
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Terrebonne, Quebec, Canada
- 502.373.0026 Centre hospitalier Pierre-Le Gardeur
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Thetford Mines, Quebec, Canada
- 502.373.0072 Chra
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Saskatchewan
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Saskatoon, Saskatchewan, Canada
- 502.373.0053 Mount Royal Clinic
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Saskatoon, Saskatchewan, Canada
- 502.373.0055 Specialists - Internal Medicine
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Saskatoon, Saskatchewan, Canada
- 502.373.0066 SDRI - University of Saskatchewan
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Saskatoon, Saskatchewan, Canada
- 502.373.0067 SDRI - University of Saskatchewan
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Saskatoon, Saskatchewan, Canada
- 502.373.0068 SDRI - University of Saskatchewan
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Saskatoon, Saskatchewan, Canada
- 502.373.0070 SDRI - University of Saskatchewan
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Aalborg, Danmark
- 502.373.1450 Boehringer Ingelheim Investigational Site
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Aarhus C, Danmark
- 502.373.1453 Boehringer Ingelheim Investigational Site
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Frederiksberg, Danmark
- 502.373.1455 Boehringer Ingelheim Investigational Site
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Frederiksberg C, Danmark
- 502.373.1459 Boehringer Ingelheim Investigational Site
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Helsingoer, Danmark
- 502.373.1460 Boehringer Ingelheim Investigational Site
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Hilleroed, Danmark
- 502.373.1458 Boehringer Ingelheim Investigational Site
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Holbaek, Danmark
- 502.373.1451 Boehringer Ingelheim Investigational Site
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Hvidovre, Danmark
- 502.373.1452 Boehringer Ingelheim Investigational Site
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Kjellerup, Danmark
- 502.373.1461 Boehringer Ingelheim Investigational Site
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Randers, Danmark
- 502.373.1456 Boehringer Ingelheim Investigational Site
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Slagelse, Danmark
- 502.373.1457 Boehringer Ingelheim Investigational Site
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Svendborg, Danmark
- 502.373.1454 Boehringer Ingelheim Investigational Site
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Moscow, Den Russiske Føderation
- 502.373.1425 Boehringer Ingelheim Investigational Site
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Moscow, Den Russiske Føderation
- 502.373.1426 Boehringer Ingelheim Investigational Site
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Moscow, Den Russiske Føderation
- 502.373.1427 Boehringer Ingelheim Investigational Site
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Moscow, Den Russiske Føderation
- 502.373.1428 Boehringer Ingelheim Investigational Site
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Moscow, Den Russiske Føderation
- 502.373.1429 Boehringer Ingelheim Investigational Site
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Moscow, Den Russiske Føderation
- 502.373.1430 Boehringer Ingelheim Investigational Site
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Moscow, Den Russiske Føderation
- 502.373.1433 Boehringer Ingelheim Investigational Site
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St. Petersburg, Den Russiske Føderation
- 502.373.1431 Boehringer Ingelheim Investigational Site
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St. Petersburg, Den Russiske Føderation
- 502.373.1432 Boehringer Ingelheim Investigational Site
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Aberdeen, Det Forenede Kongerige
- 502.373.1698 Boehringer Ingelheim Investigational Site
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Bathampton, Det Forenede Kongerige
- 502.373.1706 Boehringer Ingelheim Investigational Site
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Belfast, Det Forenede Kongerige
- 502.373.1690 Boehringer Ingelheim Investigational Site
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Birmingham, Det Forenede Kongerige
- 502.373.1694 Boehringer Ingelheim Investigational Site
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Brighton, Det Forenede Kongerige
- 502.373.1707 Boehringer Ingelheim Investigational Site
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Cardiff, Det Forenede Kongerige
- 502.373.1703 Boehringer Ingelheim Investigational Site
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Chichester, Det Forenede Kongerige
- 502.373.1709 Boehringer Ingelheim Investigational Site
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Derby, Det Forenede Kongerige
- 502.373.1701 Boehringer Ingelheim Investigational Site
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Gateshead, Det Forenede Kongerige
- 502.373.1705 Boehringer Ingelheim Investigational Site
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Glasgow, Det Forenede Kongerige
- 502.373.1710 Boehringer Ingelheim Investigational Site
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Kirkcaldy, Fife, Det Forenede Kongerige
- 502.373.1700 Boehringer Ingelheim Investigational Site
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Leeds, Det Forenede Kongerige
- 502.373.1691 Boehringer Ingelheim Investigational Site
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Leicester, Det Forenede Kongerige
- 502.373.1699 Boehringer Ingelheim Investigational Site
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Lincoln, Det Forenede Kongerige
- 502.373.1702 Boehringer Ingelheim Investigational Site
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Liverpool, Det Forenede Kongerige
- 502.373.1697 Boehringer Ingelheim Investigational Site
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London, Det Forenede Kongerige
- 502.373.1695 Boehringer Ingelheim Investigational Site
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Manchester, Det Forenede Kongerige
- 502.373.1693 Boehringer Ingelheim Investigational Site
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Portadown, County Atrim, Det Forenede Kongerige
- 502.373.1708 Boehringer Ingelheim Investigational Site
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Rugby, Det Forenede Kongerige
- 502.373.1692 Boehringer Ingelheim Investigational Site
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Sheffield, Det Forenede Kongerige
- 502.373.1696 Boehringer Ingelheim Investigational Site
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Stirling, Det Forenede Kongerige
- 502.373.1704 Boehringer Ingelheim Investigational Site
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Cavite, Filippinerne
- 502.373.0702 De La Salle University Medical Center
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Manila, Filippinerne
- 502.373.0700 Philippine General Hospital
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Manila, Filippinerne
- 502.373.0701 Manila Doctors Hospital, Room 3 Annex
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Pasig City, Filippinerne
- 502.373.0705 The Medical City
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Quezon City, Filippinerne
- 502.373.0703 Philippine Heart Center
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Quezon City, Filippinerne
- 502.373.0704 National Kidney & Transplant Institute, Room 821
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Helsinki, Finland
- 502.373.1470 Boehringer Ingelheim Investigational Site
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Helsinki, Finland
- 502.373.1473 Boehringer Ingelheim Investigational Site
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Hämeenlinna, Finland
- 502.373.1486 Boehringer Ingelheim Investigational Site
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Jyväskylä, Finland
- 502.373.1479 Boehringer Ingelheim Investigational Site
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Kuopio, Finland
- 502.373.1488 Boehringer Ingelheim Investigational Site
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Kuusankoski, Finland
- 502.373.1481 Boehringer Ingelheim Investigational Site
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Liperi, Finland
- 502.373.1487 Boehringer Ingelheim Investigational Site
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Oulun kaupunki, Finland
- 502.373.1475 Boehringer Ingelheim Investigational Site
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Turku, Finland
- 502.373.1471 Boehringer Ingelheim Investigational Site
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Vantaa, Finland
- 502.373.1485 Boehringer Ingelheim Investigational Site
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Abu Dhabi, Forenede Arabiske Emirater
- 502.373.1680 Boehringer Ingelheim Investigational Site
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Dubai, Forenede Arabiske Emirater
- 502.373.1675 Boehringer Ingelheim Investigational Site
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Dubai, Forenede Arabiske Emirater
- 502.373.1679 Boehringer Ingelheim Investigational Site
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Sharjah, Forenede Arabiske Emirater
- 502.373.1677 Boehringer Ingelheim Investigational Site
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Alabama
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Athens, Alabama, Forenede Stater
- 502.373.0256 Boehringer Ingelheim Investigational Site
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Birmingham, Alabama, Forenede Stater
- 502.373.0251 Boehringer Ingelheim Investigational Site
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Arizona
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Phoenix, Arizona, Forenede Stater
- 502.373.0182 Boehringer Ingelheim Investigational Site
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Phoenix, Arizona, Forenede Stater
- 502.373.0188 Boehringer Ingelheim Investigational Site
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Tucson, Arizona, Forenede Stater
- 502.373.0189 Boehringer Ingelheim Investigational Site
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Tuscon, Arizona, Forenede Stater
- 502.373.0177 Boehringer Ingelheim Investigational Site
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Arkansas
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Bentonville, Arkansas, Forenede Stater
- 502.373.0209 Boehringer Ingelheim Investigational Site
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California
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Concord, California, Forenede Stater
- 502.373.0173 Boehringer Ingelheim Investigational Site
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Harbor City, California, Forenede Stater
- 502.373.0266 Boehringer Ingelheim Investigational Site
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Loma Linda, California, Forenede Stater
- 502.373.0283 Boehringer Ingelheim Investigational Site
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Los Angeles, California, Forenede Stater
- 502.373.0180 Boehringer Ingelheim Investigational Site
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Sacramento, California, Forenede Stater
- 502.373.0175 Boehringer Ingelheim Investigational Site
-
San Diego, California, Forenede Stater
- 502.373.0165 Boehringer Ingelheim Investigational Site
-
San Leandro, California, Forenede Stater
- 502.373.0228 Boehringer Ingelheim Investigational Site
-
Sylmar, California, Forenede Stater
- 502.373.0205 Boehringer Ingelheim Investigational Site
-
West Hills, California, Forenede Stater
- 502.373.0277 Boehringer Ingelheim Investigational Site
-
-
Connecticut
-
Bridgeport, Connecticut, Forenede Stater
- 502.373.0226 Boehringer Ingelheim Investigational Site
-
Farmington, Connecticut, Forenede Stater
- 502.373.0174 Boehringer Ingelheim Investigational Site
-
-
District of Columbia
-
Washington, District of Columbia, Forenede Stater
- 502.373.0258 Boehringer Ingelheim Investigational Site
-
-
Florida
-
Gainesville, Florida, Forenede Stater
- 502.373.0179 Boehringer Ingelheim Investigational Site
-
Palm Harbor, Florida, Forenede Stater
- 502.373.0183 Boehringer Ingelheim Investigational Site
-
Panama City, Florida, Forenede Stater
- 502.373.0240 Boehringer Ingelheim Investigational Site
-
Tampa, Florida, Forenede Stater
- 502.373.0171 Boehringer Ingelheim Investigational Site
-
Vero Beach, Florida, Forenede Stater
- 502.373.0282 Boehringer Ingelheim Investigational Site
-
Weston, Florida, Forenede Stater
- 502.373.0214 Boehringer Ingelheim Investigational Site
-
-
Georgia
-
Augusta, Georgia, Forenede Stater
- 502.373.0161 Boehringer Ingelheim Investigational Site
-
Augusta, Georgia, Forenede Stater
- 502.373.0193 Boehringer Ingelheim Investigational Site
-
Augusta, Georgia, Forenede Stater
- 502.373.0201 Boehringer Ingelheim Investigational Site
-
Conyers, Georgia, Forenede Stater
- 502.373.0223 Boehringer Ingelheim Investigational Site
-
Sandersville, Georgia, Forenede Stater
- 502.373.0268 Boehringer Ingelheim Investigational Site
-
Savannah, Georgia, Forenede Stater
- 502.373.0245 Boehringer Ingelheim Investigational Site
-
Tucker, Georgia, Forenede Stater
- 502.373.0199 Boehringer Ingelheim Investigational Site
-
Valdosta, Georgia, Forenede Stater
- 502.373.0162 Boehringer Ingelheim Investigational Site
-
-
Idaho
-
Pocatello, Idaho, Forenede Stater
- 502.373.0203 Boehringer Ingelheim Investigational Site
-
-
Illinois
-
Burbank, Illinois, Forenede Stater
- 502.373.0244 Boehringer Ingelheim Investigational Site
-
Chicago, Illinois, Forenede Stater
- 502.373.0272 Boehringer Ingelheim Investigational Site
-
Olympia Fields, Illinois, Forenede Stater
- 502.373.0217 Boehringer Ingelheim Investigational Site
-
-
Iowa
-
Des Moines, Iowa, Forenede Stater
- 502.373.0270 Boehringer Ingelheim Investigational Site
-
-
Louisiana
-
Monroe, Louisiana, Forenede Stater
- 502.373.0167 Boehringer Ingelheim Investigational Site
-
Shreveport, Louisiana, Forenede Stater
- 502.373.0158 Boehringer Ingelheim Investigational Site
-
-
Maryland
-
Baltimore, Maryland, Forenede Stater
- 502.373.0247 Boehringer Ingelheim Investigational Site
-
-
Massachusetts
-
Boston, Massachusetts, Forenede Stater
- 502.373.0284 Boehringer Ingelheim Investigational Site
-
Springfield, Massachusetts, Forenede Stater
- 502.373.0229 Boehringer Ingelheim Investigational Site
-
-
Michigan
-
Wyandotte, Michigan, Forenede Stater
- 502.373.0237 Boehringer Ingelheim Investigational Site
-
-
Minnesota
-
Minneapolis, Minnesota, Forenede Stater
- 502.373.0208 Boehringer Ingelheim Investigational Site
-
Minneapolis, Minnesota, Forenede Stater
- 502.373.0232 Boehringer Ingelheim Investigational Site
-
St. Paul, Minnesota, Forenede Stater
- 502.373.0231 Boehringer Ingelheim Investigational Site
-
-
Mississippi
-
Biloxi, Mississippi, Forenede Stater
- 502.373.0181 Boehringer Ingelheim Investigational Site
-
Cleveland, Mississippi, Forenede Stater
- 502.373.0185 Boehringer Ingelheim Investigational Site
-
Jackson, Mississippi, Forenede Stater
- 502.373.0254 Boehringer Ingelheim Investigational Site
-
-
Missouri
-
Kansas City, Missouri, Forenede Stater
- 502.373.0195 Boehringer Ingelheim Investigational Site
-
St. Louis, Missouri, Forenede Stater
- 502.373.0207 Boehringer Ingelheim Investigational Site
-
St. Louis, Missouri, Forenede Stater
- 502.373.0239 Boehringer Ingelheim Investigational Site
-
-
Nebraska
-
Omaha, Nebraska, Forenede Stater
- 502.373.0279 Boehringer Ingelheim Investigational Site
-
-
Nevada
-
North Las Vegas, Nevada, Forenede Stater
- 502.373.0169 Boehringer Ingelheim Investigational Site
-
-
New Jersey
-
Camden, New Jersey, Forenede Stater
- 502.373.0157 Boehringer Ingelheim Investigational Site
-
East Orange, New Jersey, Forenede Stater
- 502.373.0202 Boehringer Ingelheim Investigational Site
-
Newark, New Jersey, Forenede Stater
- 502.373.0191 Boehringer Ingelheim Investigational Site
-
Westwood, New Jersey, Forenede Stater
- 502.373.0271 Boehringer Ingelheim Investigational Site
-
-
New York
-
Bronx, New York, Forenede Stater
- 502.373.0150 Boehringer Ingelheim Investigational Site
-
Brooklyn, New York, Forenede Stater
- 502.373.0213 Boehringer Ingelheim Investigational Site
-
Buffalo, New York, Forenede Stater
- 502.373.0230 Boehringer Ingelheim Investigational Site
-
Kingston, New York, Forenede Stater
- 502.373.0288 Boehringer Ingelheim Investigational Site
-
New York, New York, Forenede Stater
- 502.373.0238 Boehringer Ingelheim Investigational Site
-
New York, New York, Forenede Stater
- 502.373.0252 Boehringer Ingelheim Investigational Site
-
New York, New York, Forenede Stater
- 502.373.0286 Boehringer Ingelheim Investigational Site
-
Northport, New York, Forenede Stater
- 502.373.0166 Boehringer Ingelheim Investigational Site
-
Rochester, New York, Forenede Stater
- 502.373.0156 Boehringer Ingelheim Investigational Site
-
Rochester, New York, Forenede Stater
- 502.373.0264 Boehringer Ingelheim Investigational Site
-
Scarsdale, New York, Forenede Stater
- 502.373.0227 Boehringer Ingelheim Investigational Site
-
Westfield, New York, Forenede Stater
- 502.373.0163 Boehringer Ingelheim Investigational Site
-
Williamsville, New York, Forenede Stater
- 502.373.0241 Boehringer Ingelheim Investigational Site
-
-
North Carolina
-
Durham, North Carolina, Forenede Stater
- 502.373.0273 Boehringer Ingelheim Investigational Site
-
Winston Salem, North Carolina, Forenede Stater
- 502.373.0261 Boehringer Ingelheim Investigational Site
-
-
North Dakota
-
Fargo, North Dakota, Forenede Stater
- 502.373.0222 Boehringer Ingelheim Investigational Site
-
-
Ohio
-
Cincinnati, Ohio, Forenede Stater
- 502.373.0155 Boehringer Ingelheim Investigational Site
-
Cleveland, Ohio, Forenede Stater
- 502.373.0164 Boehringer Ingelheim Investigational Site
-
Dayton, Ohio, Forenede Stater
- 502.373.0168 Boehringer Ingelheim Investigational Site
-
Mansfield, Ohio, Forenede Stater
- 502.373.0159 Boehringer Ingelheim Investigational Site
-
Oklahoma City, Ohio, Forenede Stater
- 502.373.0178 Boehringer Ingelheim Investigational Site
-
-
Oklahoma
-
Guthrie, Oklahoma, Forenede Stater
- 502.373.0259 Boehringer Ingelheim Investigational Site
-
Oklahoma City, Oklahoma, Forenede Stater
- 502.373.0154 Boehringer Ingelheim Investigational Site
-
Tulsa, Oklahoma, Forenede Stater
- 502.373.0152 Boehringer Ingelheim Investigational Site
-
-
Oregon
-
Portland, Oregon, Forenede Stater
- 502.373.0243 Boehringer Ingelheim Investigational Site
-
-
Pennsylvania
-
Erie, Pennsylvania, Forenede Stater
- 502.373.0265 Boehringer Ingelheim Investigational Site
-
Philadelphia, Pennsylvania, Forenede Stater
- 502.373.0153 Boehringer Ingelheim Investigational Site
-
Sellersville, Pennsylvania, Forenede Stater
- 502.373.0274 Boehringer Ingelheim Investigational Site
-
-
South Carolina
-
Charleston, South Carolina, Forenede Stater
- 502.373.0184 Boehringer Ingelheim Investigational Site
-
Columbia, South Carolina, Forenede Stater
- 502.373.0248 Boehringer Ingelheim Investigational Site
-
-
Texas
-
Dallas, Texas, Forenede Stater
- 502.373.0172 Boehringer Ingelheim Investigational Site
-
Dallas, Texas, Forenede Stater
- 502.373.0187 Boehringer Ingelheim Investigational Site
-
Dallas, Texas, Forenede Stater
- 502.373.0219 Boehringer Ingelheim Investigational Site
-
Dallas, Texas, Forenede Stater
- 502.373.0275 Boehringer Ingelheim Investigational Site
-
Fort Worth, Texas, Forenede Stater
- 502.373.0221 Boehringer Ingelheim Investigational Site
-
Houston, Texas, Forenede Stater
- 502.373.0206 Boehringer Ingelheim Investigational Site
-
Houston, Texas, Forenede Stater
- 502.373.0234 Boehringer Ingelheim Investigational Site
-
Houston, Texas, Forenede Stater
- 502.373.0280 Boehringer Ingelheim Investigational Site
-
-
Virginia
-
Burke, Virginia, Forenede Stater
- 502.373.0249 Boehringer Ingelheim Investigational Site
-
-
Washington
-
Seattle, Washington, Forenede Stater
- 502.373.0281 Boehringer Ingelheim Investigational Site
-
-
Wisconsin
-
Milwaukee, Wisconsin, Forenede Stater
- 502.373.0212 Boehringer Ingelheim Investigational Site
-
-
-
-
-
Albens, Frankrig
- 502.373.1093 Cabinet Médical
-
Beziers, Frankrig
- 502.373.1090 Cabinet Médical
-
Bourges, Frankrig
- 502.373.1075 Cabinet Médical
-
Broglie, Frankrig
- 502.373.1091 Cabinet Médical
-
Castelnaudary, Frankrig
- 502.373.1097 Cabinet Médical
-
Gemenos, Frankrig
- 502.373.1089 Cabinet Médical
-
Husseren Wesserlin, Frankrig
- 502.373.1099 Cabinet Médical
-
Hyeres, Frankrig
- 502.373.1094 Cabinet Médical
-
L'Aigle, Frankrig
- 502.373.1078 Cabinet Médical des Tanneurs
-
La Rochelle, Frankrig
- 502.373.1096 Cabinet Médical
-
Le Pradet, Frankrig
- 502.373.1081 Cabinet Médical
-
Murs Erigne, Frankrig
- 502.373.1083 Cabinet Médical
-
Nantes, Frankrig
- 502.373.1084 Cabinet Médical
-
Nantes, Frankrig
- 502.373.1086 Cabinet Médical
-
Niort, Frankrig
- 502.373.1080 Cabinet Médical
-
Ortez, Frankrig
- 502.373.1095 Cabinet Médical
-
Paris, Frankrig
- 502.373.1079 Cabinet Médical
-
Rennes, Frankrig
- 502.373.1088 Cabinet Médical
-
Rosiers d'Egletons, Frankrig
- 502.373.1098 Cabinet Médical
-
Saint Julien des Landes, Frankrig
- 502.373.1085 Cabinet Médical
-
Saint Martin dHyeres, Frankrig
- 502.373.1076 Cabinet Médical La Grande Ramée
-
Saint Pierre de Chandieu, Frankrig
- 502.373.1092 Cabinet Médical de St Pierre
-
Saint Romain sur Cher, Frankrig
- 502.373.1077 Cabinet Médical
-
Strasbourg, Frankrig
- 502.373.1087 Cabinet Médical
-
Tours, Frankrig
- 502.373.1082 Cabinet Médical
-
-
-
-
-
Athens, Grækenland
- 502.373.1200 Boehringer Ingelheim Investigational Site
-
Athens, Grækenland
- 502.373.1203 Boehringer Ingelheim Investigational Site
-
Athens, Grækenland
- 502.373.1206 Boehringer Ingelheim Investigational Site
-
Athens, Grækenland
- 502.373.1207 Boehringer Ingelheim Investigational Site
-
Athens, Grækenland
- 502.373.1208 Boehringer Ingelheim Investigational Site
-
Athens, Grækenland
- 502.373.1214 Boehringer Ingelheim Investigational Site
-
Elefsina, Grækenland
- 502.373.1209 Boehringer Ingelheim Investigational Site
-
Goudi/ Athens, Grækenland
- 502.373.1211 Boehringer Ingelheim Investigational Site
-
Ioannina, Grækenland
- 502.373.1201 Boehringer Ingelheim Investigational Site
-
Kavala,greece, Grækenland
- 502.373.1210 Boehringer Ingelheim Investigational Site
-
Korinthos, Grækenland
- 502.373.1224 Boehringer Ingelheim Investigational Site
-
Melissia, Athens, Grækenland
- 502.373.1202 Boehringer Ingelheim Investigational Site
-
Thessaloniki, Grækenland
- 502.373.1205 Boehringer Ingelheim Investigational Site
-
Thessaloniki, Grækenland
- 502.373.1213 Boehringer Ingelheim Investigational Site
-
Veria, Grækenland
- 502.373.1204 Boehringer Ingelheim Investigational Site
-
-
-
-
-
Amsterdam, Holland
- 502.373.1309 Boehringer Ingelheim Investigational Site
-
Beverwijk, Holland
- 502.373.1305 Boehringer Ingelheim Investigational Site
-
Den Bosch, Holland
- 502.373.1313 Boehringer Ingelheim Investigational Site
-
Den Haag, Holland
- 502.373.1312 Boehringer Ingelheim Investigational Site
-
Doetinchem, Holland
- 502.373.1302 Boehringer Ingelheim Investigational Site
-
Drachten, Holland
- 502.373.1304 Boehringer Ingelheim Investigational Site
-
Eindhoven, Holland
- 502.373.1301 Boehringer Ingelheim Investigational Site
-
Ermelo, Holland
- 502.373.1318 Boehringer Ingelheim Investigational Site
-
Ewijk, Holland
- 502.373.1320 Boehringer Ingelheim Investigational Site
-
Hengelo, Holland
- 502.373.1310 Boehringer Ingelheim Investigational Site
-
Hoorn, Holland
- 502.373.1303 Boehringer Ingelheim Investigational Site
-
Huizen, Holland
- 502.373.1322 Boehringer Ingelheim Investigational Site
-
Lichtenvoorde, Holland
- 502.373.1300 Boehringer Ingelheim Investigational Site
-
Losser, Holland
- 502.373.1323 Boehringer Ingelheim Investigational Site
-
Nieuwegein, Holland
- 502.373.1307 Boehringer Ingelheim Investigational Site
-
Rijswijk, Holland
- 502.373.1317 Boehringer Ingelheim Investigational Site
-
Roelofarendsveen, Holland
- 502.373.1319 Boehringer Ingelheim Investigational Site
-
Rotterdam, Holland
- 502.373.1308 Boehringer Ingelheim Investigational Site
-
Spijkenisse, Holland
- 502.373.1321 Boehringer Ingelheim Investigational Site
-
Stadskanaal, Holland
- 502.373.1311 Boehringer Ingelheim Investigational Site
-
Tilburg, Holland
- 502.373.1314 Boehringer Ingelheim Investigational Site
-
Utrecht, Holland
- 502.373.1316 Boehringer Ingelheim Investigational Site
-
Velp, Holland
- 502.373.1315 Boehringer Ingelheim Investigational Site
-
-
-
-
-
Hong Kong, Hong Kong
- 502.373.0676 Boehringer Ingelheim Investigational Site
-
Hong Kong, Hong Kong
- 502.373.0677 Boehringer Ingelheim Investigational Site
-
Hong Kong, Hong Kong
- 502.373.0680 Boehringer Ingelheim Investigational Site
-
Hong Kong, Hong Kong
- 502.373.0681 Boehringer Ingelheim Investigational Site
-
Hong Kong, Hong Kong
- 502.373.0685 Boehringer Ingelheim Investigational Site
-
-
-
-
-
Dublin 24, Irland
- 502.373.1717 Adelaide & Meath Hospitals
-
Dublin 8, Irland
- 502.373.1714 Dept. of Clinical Pharmacology
-
Dublin 9, Irland
- 502.373.1719 Pulmonary Function Laboratory
-
Mallow, Irland
- 502.373.1720 Mallow General Hospital
-
-
-
-
-
Ascoli Piceno, Italien
- 502.373.1257 Ospedale "Mazzoni"
-
Bentivoglio (BO), Italien
- 502.373.1259 Ospedale di Bentivoglio
-
Bologna, Italien
- 502.373.1255 Ospedale "S. Orsola Malpighi"
-
Bologna, Italien
- 502.373.1278 Ospedale Bellaria
-
Brescia, Italien
- 502.373.1275 A.O. Spedali Civili di Brescia -Univ. degli studi di Brescia
-
Casarano (LE), Italien
- 502.373.1261 Ospedale Civile di Casarano
-
Caserta, Italien
- 502.373.1252 Azienda Ospedaliera di Caserta
-
Città della Pieve (PG), Italien
- 502.373.1254 Ospedale di Città della Pieve
-
Ferrara, Italien
- 502.373.1262 Arcispedale "S. Anna"
-
Monfalcone (go), Italien
- 502.373.1250 Ospedale Civile "S. Polo"
-
Napoli, Italien
- 502.373.1266 Azienda Universitaria Policlinico "Federico II"
-
Napoli, Italien
- 502.373.1267 Azienda Universitaria Policlinico II
-
Napoli, Italien
- 502.373.1269 Università Federico II
-
Napoli, Italien
- 502.373.1279 Asl Na 1
-
Palermo, Italien
- 502.373.1264 Presidio Ospedaliero "Villa Sofia"
-
Pavia, Italien
- 502.373.1265 IRCCS - Policlinico S. Matteo
-
Perugia, Italien
- 502.373.1251 Policlinico Monteluce
-
Perugia, Italien
- 502.373.1258 Ospedale "R. Silvestrini"
-
Perugia, Italien
- 502.373.1274 Ospedale "R. Silvestrini"
-
Pozzilli (IS), Italien
- 502.373.1253 Istituto di Ricovero a Carattere Scientifico Neuromed- IRCCS
-
Roma, Italien
- 502.373.1263 Policlinico Umberto I
-
Roma, Italien
- 502.373.1268 Ospedale "S. Spirito"
-
Roma, Italien
- 502.373.1270 Policlinico di Tor Vergata
-
Roma, Italien
- 502.373.1273 A.O. "S. Camillo de Lellis"
-
S. Pietro Vernotico (BR), Italien
- 502.373.1260 Ospedale "N. Melli"
-
Sassari, Italien
- 502.373.1256 Ospedale Civile SS. Annunziata - USL 1
-
Torino, Italien
- 502.373.1277 A.S.O. "S. Giovanni Battista"
-
Varese, Italien
- 502.373.1272 Ospedale di Circolo di Varese
-
Venezia, Italien
- 502.373.1271 Ospedale Civile
-
Viterbo, Italien
- 502.373.1276 Ospedale Belcolle
-
-
-
-
-
Adana, Kalkun
- 502.373.1651 Cukurova Universitesi Tip Fakultesi
-
Adana, Kalkun
- 502.373.1652 Cukurova Universitesi Tip Fakultesi
-
Ankara, Kalkun
- 502.373.1653 Ankara Hastanesi Endokrinoloji Bölümü
-
Ankara, Kalkun
- 502.373.1656 Baskent Universitesi Tip Fakultesi
-
Ankara, Kalkun
- 502.373.1659 Ankara Universitesi Tip Fakultesi
-
Istanbul, Kalkun
- 502.373.1654 Göztepe SSK Egitim ve Arastirma Hastanesi
-
Istanbul, Kalkun
- 502.373.1655 Cerrahpasa Universitesi Tip Fakultesi
-
Istanbul, Kalkun
- 502.373.1657 Haseki Hastanesi
-
Izmir, Kalkun
- 502.373.1658 Ege Universitesi Tip Fakultesi
-
Kayseri, Kalkun
- 502.373.1650 Erciyes Universitesi Tip Fakultesi Kardiyoloji Anabilim Dali
-
-
-
-
-
Beijing, Kina
- 502.373.0601 Boehringer Ingelheim Investigational Site
-
Beijing, Kina
- 502.373.0602 Boehringer Ingelheim Investigational Site
-
Beijing, Kina
- 502.373.0603 Boehringer Ingelheim Investigational Site
-
Beijing, Kina
- 502.373.0604 Boehringer Ingelheim Investigational Site
-
Beijing, Kina
- 502.373.0605 Boehringer Ingelheim Investigational Site
-
Beijing, Kina
- 502.373.0606 Boehringer Ingelheim Investigational Site
-
Beijing, Kina
- 502.373.0607 Boehringer Ingelheim Investigational Site
-
Beijing, Kina
- 502.373.0621 Boehringer Ingelheim Investigational Site
-
Beijing, Kina
- 502.373.0622 Boehringer Ingelheim Investigational Site
-
Beijing, Kina
- 502.373.0623 Boehringer Ingelheim Investigational Site
-
Beijing, Kina
- 502.373.0626 Boehringer Ingelheim Investigational Site
-
Changsha, Kina
- 502.373.0616 Boehringer Ingelheim Investigational Site
-
Chengdu, Kina
- 502.373.0613 Boehringer Ingelheim Investigational Site
-
Chengdu, Kina
- 502.373.0625 Boehringer Ingelheim Investigational Site
-
Guangzhou, Kina
- 502.373.0620 Boehringer Ingelheim Investigational Site
-
Harbin, Kina
- 502.373.0612 Boehringer Ingelheim Investigational Site
-
HeBei Province, Kina
- 502.373.0634 Boehringer Ingelheim Investigational Site
-
Henan Province, Kina
- 502.373.0624 Boehringer Ingelheim Investigational Site
-
Hubei Province, Kina
- 502.373.0627 Boehringer Ingelheim Investigational Site
-
Nanjing, Kina
- 502.373.0614 Boehringer Ingelheim Investigational Site
-
QingDao, Kina
- 502.373.0629 Boehringer Ingelheim Investigational Site
-
ShanDong Province, Kina
- 502.373.0632 Boehringer Ingelheim Investigational Site
-
ShanDong Province, Kina
- 502.373.0633 Boehringer Ingelheim Investigational Site
-
Shanghai, Kina
- 502.373.0617 Boehringer Ingelheim Investigational Site
-
Shanghai, Kina
- 502.373.0618 Boehringer Ingelheim Investigational Site
-
Shanghai, Kina
- 502.373.0619 Boehringer Ingelheim Investigational Site
-
Shen Yang, Kina
- 502.373.0628 Boehringer Ingelheim Investigational Site
-
Shijiazhuang, Kina
- 502.373.0611 Boehringer Ingelheim Investigational Site
-
Tianjin, Kina
- 502.373.0615 Boehringer Ingelheim Investigational Site
-
Tianjin, Kina
- 502.373.0631 Boehringer Ingelheim Investigational Site
-
Weizikeng, Kina
- 502.373.0630 Boehringer Ingelheim Investigational Site
-
Wuhan, Kina
- 502.373.0608 Boehringer Ingelheim Investigational Site
-
Zhenzhou, Kina
- 502.373.0610 Boehringer Ingelheim Investigational Site
-
-
-
-
-
Incheon, Korea, Republikken
- 502.373.0763 Boehringer Ingelheim Investigational Site
-
Kwang-ju, Korea, Republikken
- 502.373.0764 Boehringer Ingelheim Investigational Site
-
Pusan, Korea, Republikken
- 502.373.0755 Boehringer Ingelheim Investigational Site
-
Seoul, Korea, Republikken
- 502.373.0750 Boehringer Ingelheim Investigational Site
-
Seoul, Korea, Republikken
- 502.373.0753 Boehringer Ingelheim Investigational Site
-
Seoul, Korea, Republikken
- 502.373.0756 Boehringer Ingelheim Investigational Site
-
Seoul, Korea, Republikken
- 502.373.0757 Boehringer Ingelheim Investigational Site
-
Seoul, Korea, Republikken
- 502.373.0760 Boehringer Ingelheim Investigational Site
-
Seoul, Korea, Republikken
- 502.373.0761 Boehringer Ingelheim Investigational Site
-
Taegu, Korea, Republikken
- 502.373.0754 Boehringer Ingelheim Investigational Site
-
-
-
-
-
Johor Baharu, Malaysia
- 502.373.0736 Boehringer Ingelheim Investigational Site
-
Kelantan, Malaysia
- 502.373.0739 Boehringer Ingelheim Investigational Site
-
Kelantan Darul Naim, Malaysia
- 502.373.2707 Boehringer Ingelheim Investigational Site
-
Kuala Lumpur, Malaysia
- 502.373.0732 Boehringer Ingelheim Investigational Site
-
Kuala Lumpur, Malaysia
- 502.373.0734 Boehringer Ingelheim Investigational Site
-
Penang, Malaysia
- 502.373.0733 Boehringer Ingelheim Investigational Site
-
Putrajaya, Malaysia
- 502.373.0731 Boehringer Ingelheim Investigational Site
-
Selangor, Malaysia
- 502.373.60001 Boehringer Ingelheim Investigational Site
-
-
-
-
-
Guadalajara, Mexico
- 502.373.0450 Boehringer Ingelheim Investigational Site
-
Guadalajara, Mexico
- 502.373.0451 Boehringer Ingelheim Investigational Site
-
Guadalajara, Mexico
- 502.373.0452 Boehringer Ingelheim Investigational Site
-
Guadalajara, Mexico
- 502.373.0459 Boehringer Ingelheim Investigational Site
-
Guadalajara, Mexico
- 502.373.0460 Boehringer Ingelheim Investigational Site
-
Guadalajara, Mexico
- 502.373.0461 Boehringer Ingelheim Investigational Site
-
Guadalajara, Mexico
- 502.373.0470 Boehringer Ingelheim Investigational Site
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Mexico, Mexico
- 502.373.0457 Boehringer Ingelheim Investigational Site
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Mexico, Mexico
- 502.373.0458 Boehringer Ingelheim Investigational Site
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Monterrey, Mexico
- 502.373.0454 Boehringer Ingelheim Investigational Site
-
Zapopan, Mexico
- 502.373.0453 Boehringer Ingelheim Investigational Site
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Zapopan, Mexico
- 502.373.0456 Boehringer Ingelheim Investigational Site
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Auckland, New Zealand
- 502.373.0500 Boehringer Ingelheim Investigational Site
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Auckland 3, New Zealand
- 502.373.0502 Boehringer Ingelheim Investigational Site
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Christchurch, New Zealand
- 502.373.0507 Boehringer Ingelheim Investigational Site
-
Hamiton, New Zealand
- 502.373.0504 Boehringer Ingelheim Investigational Site
-
Hasting, New Zealand
- 502.373.0506 Boehringer Ingelheim Investigational Site
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Otahuhu Auckland, New Zealand
- 502.373.0501 Middlemore Hospital
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Takapuna Auckland, New Zealand
- 502.373.0503 Boehringer Ingelheim Investigational Site
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Tauranga, New Zealand
- 502.373.0505 Tauranga Study Centre
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Fevik, Norge
- 502.373.20003 Boehringer Ingelheim Investigational Site
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Nesttun, Norge
- 502.373.20004 Fana Hjertesenter
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Stavanger, Norge
- 502.373.20001 Stavanger Universitetssykehus
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Tvedestrand, Norge
- 502.373.20002 Tvedestrand Legesenter
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Tønsberg, Norge
- 502.373.20005 Sykehuset i Vestfold, Avd. Tønsberg
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Bydgoszcz, Polen
- 502.373.1354 Boehringer Ingelheim Investigational Site
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Czestochowa, Polen
- 502.373.1366 Boehringer Ingelheim Investigational Site
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Gdynia, Polen
- 502.373.1368 Boehringer Ingelheim Investigational Site
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Gdynia Redlowo, Polen
- 502.373.1365 Boehringer Ingelheim Investigational Site
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Grojec, Polen
- 502.373.1359 Boehringer Ingelheim Investigational Site
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Grudziadz, Polen
- 502.373.1369 Boehringer Ingelheim Investigational Site
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Inowroclaw, Polen
- 502.373.1375 Boehringer Ingelheim Investigational Site
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Jaroslawiec, Polen
- 502.373.1360 Boehringer Ingelheim Investigational Site
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Katowice, Polen
- 502.373.1372 Boehringer Ingelheim Investigational Site
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Katowice, Polen
- 502.373.1376 Boehringer Ingelheim Investigational Site
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Kielce, Polen
- 502.373.1361 Boehringer Ingelheim Investigational Site
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Lodz, Polen
- 502.373.1358 Boehringer Ingelheim Investigational Site
-
Lubartow, Polen
- 502.373.1364 Boehringer Ingelheim Investigational Site
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Lubin, Polen
- 502.373.1374 Boehringer Ingelheim Investigational Site
-
Nowy Sacz, Polen
- 502.373.1367 Boehringer Ingelheim Investigational Site
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Piotrkow Trybunalski, Polen
- 502.373.1356 Boehringer Ingelheim Investigational Site
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Poznan, Polen
- 502.373.1370 Boehringer Ingelheim Investigational Site
-
Ruda Slaska, Polen
- 502.373.1357 Boehringer Ingelheim Investigational Site
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Skierniewice, Polen
- 502.373.1352 Boehringer Ingelheim Investigational Site
-
Tarnow, Polen
- 502.373.1362 Boehringer Ingelheim Investigational Site
-
Tomaszow Mazowiecki, Polen
- 502.373.1355 Boehringer Ingelheim Investigational Site
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Torun, Polen
- 502.373.1353 Boehringer Ingelheim Investigational Site
-
Warsaw, Polen
- 502.373.1351 Boehringer Ingelheim Investigational Site
-
Warsaw, Polen
- 502.373.1363 Boehringer Ingelheim Investigational Site
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Wegrow, Polen
- 502.373.1373 Boehringer Ingelheim Investigational Site
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Almada, Portugal
- 502.373.1402 Hospital Garcia de Orta
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Amadora, Portugal
- 502.373.1400 Hospital Fernando Fonseca
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Carnaxide, Portugal, 2799-523
- 502.373.1411 Hospital de Santa Cruz
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Coimbra, Portugal
- 502.373.1408 Hospitais da Universidade de Coimbra
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Faro, Portugal
- 502.373.1406 Hospital Distrital de Faro Geral
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Lisboa, Portugal
- 502.373.1403 Hospital de Santa Marta
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Lisboa, Portugal
- 502.373.1409 Hospital de Santa Maria
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Matosinhos, Portugal
- 502.373.1401 Unidade Local de Saúde de Matosinhos
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Porto, Portugal
- 502.373.1410 Hospital de Santo António
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Vila Nova de Gaia, Portugal
- 502.373.1407 Centro Hospitalar vila Nova de Gaia
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Caguas, Puerto Rico
- 502.373.0215 Boehringer Ingelheim Investigational Site
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Las Lomas, Puerto Rico
- 502.373.0267 Boehringer Ingelheim Investigational Site
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Manati, Puerto Rico
- 502.373.0190 Boehringer Ingelheim Investigational Site
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Orocovis, Puerto Rico
- 502.373.0198 Boehringer Ingelheim Investigational Site
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Rio Piedras, Puerto Rico
- 502.373.0262 Boehringer Ingelheim Investigational Site
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Basel, Schweiz
- 502.373.1625 Boehringer Ingelheim Investigational Site
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Bellinzona, Schweiz
- 502.373.1632 Boehringer Ingelheim Investigational Site
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Bern, Schweiz
- 502.373.1634 Boehringer Ingelheim Investigational Site
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Biel/Bienne, Schweiz
- 502.373.1627 Boehringer Ingelheim Investigational Site
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Chur, Schweiz
- 502.373.1631 Boehringer Ingelheim Investigational Site
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Kreuzlingen, Schweiz
- 502.373.1633 Boehringer Ingelheim Investigational Site
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Lausanne, Schweiz
- 502.373.1639 Boehringer Ingelheim Investigational Site
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Lugano, Schweiz
- 502.373.1629 Boehringer Ingelheim Investigational Site
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St. Gallen, Schweiz
- 502.373.1628 Boehringer Ingelheim Investigational Site
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Zürich, Schweiz
- 502.373.1637 Boehringer Ingelheim Investigational Site
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Kuala Lumpur, Singapore
- 502.373.2706 Boehringer Ingelheim Investigational Site
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Singapore, Singapore
- 502.373.0725 Boehringer Ingelheim Investigational Site
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Singapore, Singapore
- 502.373.0726 Boehringer Ingelheim Investigational Site
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Bratislava, Slovakiet
- 502.373.1535 Boehringer Ingelheim Investigational Site
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Kosice, Slovakiet
- 502.373.1529 Boehringer Ingelheim Investigational Site
-
Kosice, Slovakiet
- 502.373.1540 Boehringer Ingelheim Investigational Site
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Nitra, Slovakiet
- 502.373.1538 Boehringer Ingelheim Investigational Site
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Rimavska Sobota, Slovakiet
- 502.373.1545 Boehringer Ingelheim Investigational Site
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-
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Alcorcón (Madrid), Spanien
- 502.373.1582 Boehringer Ingelheim Investigational Site
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Alicante, Spanien
- 502.373.1601 Boehringer Ingelheim Investigational Site
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Barcelona, Spanien
- 502.373.1586 Boehringer Ingelheim Investigational Site
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Barcelona, Spanien
- 502.373.1590 Boehringer Ingelheim Investigational Site
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Barcelona, Spanien
- 502.373.1597 Boehringer Ingelheim Investigational Site
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Barcelona, Spanien
- 502.373.1599 Boehringer Ingelheim Investigational Site
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Burjasot (Valencia), Spanien
- 502.373.1595 Boehringer Ingelheim Investigational Site
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Granada, Spanien
- 502.373.1584 Boehringer Ingelheim Investigational Site
-
Granada, Spanien
- 502.373.1585 Boehringer Ingelheim Investigational Site
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Madrid, Spanien
- 502.373.1576 Boehringer Ingelheim Investigational Site
-
Madrid, Spanien
- 502.373.1578 Boehringer Ingelheim Investigational Site
-
Madrid, Spanien
- 502.373.1580 Boehringer Ingelheim Investigational Site
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Madrid, Spanien
- 502.373.1589 Boehringer Ingelheim Investigational Site
-
Madrid, Spanien
- 502.373.1592 Boehringer Ingelheim Investigational Site
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Murcia, Spanien
- 502.373.1594 Boehringer Ingelheim Investigational Site
-
Málaga, Spanien
- 502.373.1577 Boehringer Ingelheim Investigational Site
-
Málaga, Spanien
- 502.373.1596 Boehringer Ingelheim Investigational Site
-
Santiago de Compostela, Spanien
- 502.373.1579 Boehringer Ingelheim Investigational Site
-
Santiago de Compostela, Spanien
- 502.373.1593 Boehringer Ingelheim Investigational Site
-
Santiago de Compostela, Spanien
- 502.373.1598 Boehringer Ingelheim Investigational Site
-
Sevilla, Spanien
- 502.373.1583 Boehringer Ingelheim Investigational Site
-
Valencia, Spanien
- 502.373.1575 Boehringer Ingelheim Investigational Site
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Valencia, Spanien
- 502.373.1591 Boehringer Ingelheim Investigational Site
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Göteborg, Sverige
- 502.373.1504 Capio Lundby sjukhus
-
Göteborg, Sverige
- 502.373.1509 Hjärtsektionen / Med.kliniken
-
Göteborg, Sverige
- 502.373.1514 Hjärt/Kärlforskn.enheten
-
Helsingborg, Sverige
- 502.373.1501 Hjaertmottagningen
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Järfälla, Sverige
- 502.373.1505 Jakobsbergs sjukhus
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Malmoe, Sverige
- 502.373.1502 Borgmästargaardens Läkarmottagning
-
Malmö, Sverige
- 502.373.1506 Hjärtmottagningen
-
Malmö, Sverige
- 502.373.1507 Kardiologiska kliniken
-
Malmö, Sverige
- 502.373.1508 Kolgahuset Läkargrupp
-
Sjuntorp, Sverige
- 502.373.1511 Sjuntorps Vaardcentral
-
Trollhättan, Sverige
- 502.373.1503 Källtorps Vaardcentral
-
Vännäs, Sverige
- 502.373.1512 Vännäs Vaardcentral
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-
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Bellville, Sydafrika
- 502.373.1553 Boehringer Ingelheim Investigational Site
-
Bloemfontein, Sydafrika
- 502.373.1552 Boehringer Ingelheim Investigational Site
-
Cape Town, Sydafrika
- 502.373.1550 Boehringer Ingelheim Investigational Site
-
Cape Town, Sydafrika
- 502.373.1561 Boehringer Ingelheim Investigational Site
-
Congella, Sydafrika
- 502.373.1554 Boehringer Ingelheim Investigational Site
-
Durban, Sydafrika
- 502.373.1551 Boehringer Ingelheim Investigational Site
-
Fiachrdtpark, Bloemfontein, Sydafrika
- 502.373.1560 Boehringer Ingelheim Investigational Site
-
George East, Sydafrika
- 502.373.1563 Boehringer Ingelheim Investigational Site
-
Park Town West, Sydafrika
- 502.373.1555 Boehringer Ingelheim Investigational Site
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Port Elizabeth, Sydafrika
- 502.373.1559 Boehringer Ingelheim Investigational Site
-
Port Elizabeth, Sydafrika
- 502.373.1562 Boehringer Ingelheim Investigational Site
-
Soweto, Sydafrika
- 502.373.1558 Boehringer Ingelheim Investigational Site
-
Sunninghill, Sydafrika
- 502.373.1557 Boehringer Ingelheim Investigational Site
-
Sunninghill, Sydafrika
- 502.373.1564 Boehringer Ingelheim Investigational Site
-
Vanderbijlpark, Sydafrika
- 502.373.1556 Boehringer Ingelheim Investigational Site
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-
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Changhua, Taiwan
- 502.373.0780 Boehringer Ingelheim Investigational Site
-
Chia-Yi, Taiwan
- 502.373.0779 Boehringer Ingelheim Investigational Site
-
Hualien, Taiwan
- 502.373.0783 Boehringer Ingelheim Investigational Site
-
Kaohsiung, Taiwan
- 502.373.0776 Boehringer Ingelheim Investigational Site
-
Kaohsiung, Taiwan
- 502.373.0778 Boehringer Ingelheim Investigational Site
-
Tainan, Taiwan
- 502.373.0775 Boehringer Ingelheim Investigational Site
-
Tainan, Taiwan
- 502.373.0777 Boehringer Ingelheim Investigational Site
-
Taipei, Taiwan
- 502.373.0781 Boehringer Ingelheim Investigational Site
-
Taipei, Taiwan
- 502.373.0782 Boehringer Ingelheim Investigational Site
-
-
-
-
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Bangkok, Thailand
- 502.373.0801 Boehringer Ingelheim Investigational Site
-
Bangkok, Thailand
- 502.373.0802 Boehringer Ingelheim Investigational Site
-
Bangkok, Thailand
- 502.373.0804 Boehringer Ingelheim Investigational Site
-
Bangkok, Thailand
- 502.373.0805 Boehringer Ingelheim Investigational Site
-
Bangkok, Thailand
- 502.373.0806 Boehringer Ingelheim Investigational Site
-
Bangkok, Thailand
- 502.373.0808 Boehringer Ingelheim Investigational Site
-
Khon Kaen, Thailand
- 502.373.0803 Boehringer Ingelheim Investigational Site
-
Nonthaburi, Thailand
- 502.373.0807 Boehringer Ingelheim Investigational Site
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-
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Brno, Tjekkiet
- 502.373.1053 Boehringer Ingelheim Investigational Site
-
Havirov, Tjekkiet
- 502.373.1060 Boehringer Ingelheim Investigational Site
-
Kladno, Tjekkiet
- 502.373.1055 Boehringer Ingelheim Investigational Site
-
Mlada Boleslav, Tjekkiet
- 502.373.1059 Boehringer Ingelheim Investigational Site
-
Plzen, Tjekkiet
- 502.373.1061 Boehringer Ingelheim Investigational Site
-
Prague, Tjekkiet
- 502.373.1057 Boehringer Ingelheim Investigational Site
-
Prague 5, Tjekkiet
- 502.373.1051 Boehringer Ingelheim Investigational Site
-
Praha 2, Tjekkiet
- 502.373.1062 Boehringer Ingelheim Investigational Site
-
Pribram 1, Tjekkiet
- 502.373.1056 Boehringer Ingelheim Investigational Site
-
Usti nad Orlici, Tjekkiet
- 502.373.1058 Boehringer Ingelheim Investigational Site
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Bad Lausick, Tyskland
- 502.373.1164 Boehringer Ingelheim Investigational Site
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Bad Lauterberg, Tyskland
- 502.373.1166 Boehringer Ingelheim Investigational Site
-
Bad Mergentheim, Tyskland
- 502.373.1138 Boehringer Ingelheim Investigational Site
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Berlin, Tyskland
- 502.373.1156 Boehringer Ingelheim Investigational Site
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Berlin, Tyskland
- 502.373.1160 Boehringer Ingelheim Investigational Site
-
Berlin, Tyskland
- 502.373.1161 Boehringer Ingelheim Investigational Site
-
Bielefeld, Tyskland
- 502.373.1144 Boehringer Ingelheim Investigational Site
-
Dessau, Tyskland
- 502.373.1152 Boehringer Ingelheim Investigational Site
-
Dortmund, Tyskland
- 502.373.1139 Boehringer Ingelheim Investigational Site
-
Dortmund, Tyskland
- 502.373.1159 Boehringer Ingelheim Investigational Site
-
Dresden, Tyskland
- 502.373.1136 Boehringer Ingelheim Investigational Site
-
Eberswalde, Tyskland
- 502.373.1145 Boehringer Ingelheim Investigational Site
-
Erlangen, Tyskland
- 502.373.1155 Boehringer Ingelheim Investigational Site
-
Essen, Tyskland
- 502.373.1157 Boehringer Ingelheim Investigational Site
-
Haag, Tyskland
- 502.373.1153 Boehringer Ingelheim Investigational Site
-
Hamburg, Tyskland
- 502.373.1148 Boehringer Ingelheim Investigational Site
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Heidelberg, Tyskland
- 502.373.1132 Boehringer Ingelheim Investigational Site
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Homburg/Saar, Tyskland
- 502.373.1131 Boehringer Ingelheim Investigational Site
-
Karlsburg, Tyskland
- 502.373.1147 Boehringer Ingelheim Investigational Site
-
Kelkheim, Tyskland
- 502.373.1154 Boehringer Ingelheim Investigational Site
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Köln, Tyskland
- 502.373.1137 Boehringer Ingelheim Investigational Site
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Künzing, Tyskland
- 502.373.1142 Boehringer Ingelheim Investigational Site
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Lübeck, Tyskland
- 502.373.1165 Boehringer Ingelheim Investigational Site
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Mainz, Tyskland
- 502.373.1134 Boehringer Ingelheim Investigational Site
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Melsungen, Tyskland
- 502.373.1133 Boehringer Ingelheim Investigational Site
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München, Tyskland
- 502.373.1146 Boehringer Ingelheim Investigational Site
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Offenbach am Main, Tyskland
- 502.373.1149 Boehringer Ingelheim Investigational Site
-
Riesa, Tyskland
- 502.373.1162 Boehringer Ingelheim Investigational Site
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Rostock, Tyskland
- 502.373.1140 Boehringer Ingelheim Investigational Site
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Sindelfingen, Tyskland
- 502.373.1150 Boehringer Ingelheim Investigational Site
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Starnberg, Tyskland
- 502.373.1163 Boehringer Ingelheim Investigational Site
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Stuttgart, Tyskland
- 502.373.1158 Boehringer Ingelheim Investigational Site
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Timmendorfer Strand, Tyskland
- 502.373.1167 Boehringer Ingelheim Investigational Site
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Wiesbaden, Tyskland
- 502.373.1135 Boehringer Ingelheim Investigational Site
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Witten, Tyskland
- 502.373.1141 Boehringer Ingelheim Investigational Site
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Dnyepropetrovsk, Ukraine
- 502.373.1730 Boehringer Ingelheim Investigational Site
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Dnyepropetrovsk, Ukraine
- 502.373.1731 Boehringer Ingelheim Investigational Site
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Kharkov, Ukraine
- 502.373.1728 Boehringer Ingelheim Investigational Site
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Kharkov, Ukraine
- 502.373.1732 Boehringer Ingelheim Investigational Site
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Kharkov, Ukraine
- 502.373.1733 Boehringer Ingelheim Investigational Site
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Kiev, Ukraine
- 502.373.1725 Boehringer Ingelheim Investigational Site
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Kiev, Ukraine
- 502.373.1726 Boehringer Ingelheim Investigational Site
-
Kiev, Ukraine
- 502.373.1727 Boehringer Ingelheim Investigational Site
-
Kiev, Ukraine
- 502.373.1729 Boehringer Ingelheim Investigational Site
-
Kiev, Ukraine
- 502.373.1734 Boehringer Ingelheim Investigational Site
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-
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Budapest, Ungarn
- 502.373.1227 Boehringer Ingelheim Investigational Site
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Budapest, Ungarn
- 502.373.1230 Boehringer Ingelheim Investigational Site
-
Budapest, Ungarn
- 502.373.1231 Boehringer Ingelheim Investigational Site
-
Budapest, Ungarn
- 502.373.1232 Boehringer Ingelheim Investigational Site
-
Budapest, Ungarn
- 502.373.1233 Boehringer Ingelheim Investigational Site
-
Budapest, Ungarn
- 502.373.1235 Boehringer Ingelheim Investigational Site
-
Budapest, Ungarn
- 502.373.1237 Boehringer Ingelheim Investigational Site
-
Budapest, Ungarn
- 502.373.1239 Boehringer Ingelheim Investigational Site
-
Budapest, Ungarn
- 502.373.1242 Boehringer Ingelheim Investigational Site
-
Budapest, Ungarn
- 502.373.1244 Boehringer Ingelheim Investigational Site
-
Debrecen, Ungarn
- 502.373.1236 Boehringer Ingelheim Investigational Site
-
Debrecen, Ungarn
- 502.373.1240 Boehringer Ingelheim Investigational Site
-
Kecskemet, Ungarn
- 502.373.1228 Boehringer Ingelheim Investigational Site
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Nyiregyhaza, Ungarn
- 502.373.1241 Boehringer Ingelheim Investigational Site
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Pecs, Ungarn
- 502.373.1226 Boehringer Ingelheim Investigational Site
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Siofok, Ungarn
- 502.373.1229 Boehringer Ingelheim Investigational Site
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Szeged, Ungarn
- 502.373.1238 Boehringer Ingelheim Investigational Site
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Szekesfehervar, Ungarn
- 502.373.1225 Boehringer Ingelheim Investigational Site
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Tatabanya, Ungarn
- 502.373.1234 Boehringer Ingelheim Investigational Site
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Veszprem, Ungarn
- 502.373.1243 Boehringer Ingelheim Investigational Site
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-
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Graz, Østrig
- 502.373.1128 Boehringer Ingelheim Investigational Site
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Wels, Østrig
- 502.373.1125 Boehringer Ingelheim Investigational Site
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Wien, Østrig
- 502.373.1126 Boehringer Ingelheim Investigational Site
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Wien, Østrig
- 502.373.1127 Boehringer Ingelheim Investigational Site
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Wien, Østrig
- 502.373.1129 Boehringer Ingelheim Investigational Site
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Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Beskrivelse
Inklusionskriterier:
Koronararteriesygdom: Tidligere myokardieinfarkt (> 2 dage før informeret samtykke), eller stabil eller tidligere ustabil angina (> 30 dage før informeret samtykke) med dokumenteret multikar-koronararteriesygdom eller positiv stresstest eller multikarperkutan transluminal koronar angioplastik (> 30 dage før informeret samtykke), eller tidligere koronararteriebypasstransplantation med flere kar uden angina (hvis operation udført > 4 år før informeret samtykke) eller med tilbagevendende angina efter operationen.
Anden høj risiko:
- Perifer arteriel sygdom: Tidligere bypass-operation af lemmer eller angioplastik eller amputation, claudicatio intermittens i anamnesen med ankel/arm-blodtryksforhold < 0,8 på mindst den ene side eller signifikant stenose ved angiografi eller ikke-invasiv testning
- Tidligere slagtilfælde
- Forbigående iskæmisk angreb > 7 dage og < 1 år før informeret samtykke
- Diabetes mellitus (type I eller II): med tegn på endeorganskade (retinopati, venstre ventrikelhypertrofi, mikro- eller makroalbuminuri) eller tegn på tidligere hjerte- eller karsygdomme.
Ingen bestemt og specifik indikation eller kontraindikation for nogen af undersøgelsesbehandlingerne. Skriftligt informeret samtykke.
Ekskluderingskriterier:
A. Medicinbrug:
- Manglende evne til at seponere Angiotension Converting Enzyme (ACE)-hæmmere eller Angiotension 2-receptorantagonister (AIIA'er).
- Patienter med kendt overfølsomhed eller intolerance over for angiotension 2-receptorantagonister (AIIA'er) eller angiotensionskonverterende enzym (ACE)-hæmmere.
BEMÆRK: Patienter med kendt intolerance over for angiotensionskonverterende enzymhæmmerintolerance (ACE-I) kan optages i TRANSCEND-studiet.
B. Hjerte-kar-sygdom:
- Symptomatisk kongestiv hjerteinsufficiens.
- Hæmodynamisk signifikant primær klap- eller udstrømningskanalobstruktion (f.eks. aorta- eller mitralklapstenose, asymmetrisk septalhypertrofi, defekt proteseklap).
- Konstriktiv pericarditis.
- Kompleks medfødt hjertesygdom.
- Synkopale episoder med ukendt ætiologi < 3 måneder før informeret samtykke.
- Planlagt hjerteoperation eller angioplastik inden for tre måneder.
- Ukontrolleret hypertension under behandling (dvs. blodtryk (BP) > 160/100).
- Hjertetransplantationsmodtager.
- Slagtilfælde på grund af subaraknoidal blødning
C. Andre betingelser:
Betydelig nyresygdom defineret som:
- Nyrearteriestenose;
- Kreatininclearance < 0,6 ml/min eller serumkreatinin > 265 umol/L (> 3,0 mg/dL);
- Hyperkaliæmi: kalium > 5,5 mmol/L.
- Proteinuri* (kun for TRANSCEND).
- Leverdysfunktion som defineret af følgende laboratorieparametre: Serum glutamat pyruvat transaminase( SGPT) alaninaminotransferase (ALT) eller serum glutamic oxaloeddikesyre transaminase (SGOT) aspartat aminotransferase (AST) > end 4 gange øvre grænse for normal eller yderligere kriterier for øvre leverinsufficiens normalgrænse, total bilirubin > 20 umol/L, obstruktive galdelidelser.
- Ukorrigeret volumendepletering eller natriumdepletering.
- Primær aldosteronisme.
- Arvelig fruktoseintolerance.
- Enhver anden større ikke-hjertesygdom, der forventes at reducere den forventede levetid eller forstyrre studiedeltagelsen.
- Patienten tager samtidig et andet eksperimentelt lægemiddel.
- Patient med betydelig funktionsnedsættelse, der udelukker regelmæssigt møde i klinikken til opfølgning.
- Patienten har tilstrækkelig funktionsnedsættelse eller anden inhabilitet, der udelukker regelmæssigt møde i klinikken til opfølgning.
- Kan eller ønsker ikke at give skriftligt informeret samtykke.
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: FOREBYGGELSE
- Interventionel model: PARALLEL
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
ONTARGET. Sammensat endepunkt af kardiovaskulær død, ikke-dødelig myokardieinfarkt, ikke-dødelig slagtilfælde og hospitalsindlæggelse for kongestiv hjertesvigt
Tidsramme: 56 måneder
|
Den igangværende Telmisartan Alene og kombination med Ramipril Global Endpoint-forsøg (ONTARGET).
Tid til første hændelsesanalyse af følgende definerede endepunkter, kardiovaskulær død, ikke-dødelig myokardieinfarkt, ikke-dødelig slagtilfælde og hospitalsindlæggelse for kongestiv hjertesvigt.
|
56 måneder
|
|
ONTARGET. 3-fold sammensat endepunkt for fordobling af serumkreatinin, progression til slutstadie nyresygdom (ESRD) og dødelighed af alle årsager hos patienter med diabetes nefropati
Tidsramme: 56 måneder
|
ESRD er defineret ved påbegyndelse af dialyse, behov for nyretransplantation eller eGFR <15 ml/min/1,73 m². Patienter med diabetes nefropati er diabetespatienter med makroalbuminuri vurderet som et Urin Albumin Creatinine Ratio (UACR) ≥300 mg/g Crea ved baseline. Disse nyreudfald blev ikke bedømt (bortset fra døden). |
56 måneder
|
|
TRANSCENDERE. Sammensat endepunkt af kardiovaskulær død, ikke-dødelig myokardieinfarkt, ikke-dødelig slagtilfælde og hospitalsindlæggelse for kongestiv hjertesvigt
Tidsramme: 56 måneder
|
Telmisartan Randomized Assessment Study in Angiotension Converting Enzyme Inhibitor intolerante forsøgspersoner med kardiovaskulær sygdom (TRANSCEND).
Tid til første hændelsesanalyse af følgende definerede endepunkter, kardiovaskulær død, ikke-dødelig myokardieinfarkt, ikke-dødelig slagtilfælde og hospitalsindlæggelse for kongestiv hjertesvigt.
|
56 måneder
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
ONTARGET. Sammensat endepunkt af kardiovaskulær død, ikke-dødelig myokardieinfarkt og ikke-dødelig slagtilfælde
Tidsramme: 56 måneder
|
Den igangværende Telmisartan Alene og kombination med Ramipril Global Endpoint-forsøg (ONTARGET).
Tid til første hændelsesanalyse af følgende definerede endepunkter, ikke-fatalt myokardieinfarkt eller ikke-fatalt slagtilfælde
|
56 måneder
|
|
ONTARGET. Kardiovaskulær død
Tidsramme: 56 måneder
|
Den igangværende Telmisartan Alene og kombination med Ramipril Global Endpoint-forsøg (ONTARGET).
Tid til den første hændelsesanalyse af endepunktet kardiovaskulær død.
|
56 måneder
|
|
ONTARGET. Ikke-dødelig myokardieinfarkt
Tidsramme: 56 måneder
|
Den igangværende Telmisartan Alene og kombination med Ramipril Global Endpoint-forsøg (ONTARGET).
Tid til den første hændelsesanalyse af endepunktet ikke-fatalt myokardieinfarkt.
|
56 måneder
|
|
ONTARGET. Ikke-dødelig slagtilfælde
Tidsramme: 56 måneder
|
Den igangværende Telmisartan Alene og kombination med Ramipril Global Endpoint-forsøg (ONTARGET).
Tid til første hændelsesanalyse af endepunktet ikke-dødelig slagtilfælde.
|
56 måneder
|
|
ONTARGET. Hospitalsindlæggelse for kongestiv hjertesvigt
Tidsramme: 56 måneder
|
Den igangværende Telmisartan Alene og kombination med Ramipril Global Endpoint-forsøg (ONTARGET).
Tid til den første hændelsesanalyse af endepunktet hospitalsindlæggelse for kongestiv hjertesvigt.
|
56 måneder
|
|
ONTARGET. Fordobling af serumkreatinin hos patienter med diabetes nefropati
Tidsramme: 56 måneder
|
Patienter med diabetes nefropati er diabetespatienter med makroalbuminuri vurderet som et Urin Albumin Creatinine Ratio (UACR) ≥300 mg/g Crea ved baseline.
|
56 måneder
|
|
ONTARGET. Progression til slutstadiet af nyresygdom (ESRD) hos patienter med diabetes nefropati
Tidsramme: 56 måneder
|
ESRD er defineret ved påbegyndelse af dialyse, behov for nyretransplantation eller eGFR <15 ml/min/1,73
m².
Patienter med diabetes nefropati er diabetespatienter med makroalbuminuri vurderet som et Urin Albumin Creatinine Ratio (UACR) ≥300 mg/g Crea ved baseline.
|
56 måneder
|
|
ONTARGET. Dødelighed af alle årsager hos patienter med diabetes nefropati
Tidsramme: 56 måneder
|
Patienter med diabetes nefropati er diabetespatienter med makroalbuminuri vurderet som et Urin Albumin Creatinine Ratio (UACR) ≥300 mg/g Crea ved baseline.
|
56 måneder
|
|
ONTARGET. Fordobling af serumkreatinin
Tidsramme: 56 måneder
|
ONTARGET.
Nefropati underkategori: fordobling af serumkreatinin
|
56 måneder
|
|
ONTARGET. Progression til ESRD
Tidsramme: 56 måneder
|
ONTARGET.
Nefropati underkategori: Progression til ESRD.
Progression til ESRD er defineret som påbegyndelse af dialyse, behov for nyretransplantation eller eGFR <15 ml/min/1,73
m².
|
56 måneder
|
|
ONTARGET. Ny mikroalbuminuri
Tidsramme: 56 måneder
|
ONTARGET.
Nefropati underkategori: Ny mikroalbuminuri.
Ny mikroalbuminuri er defineret som Urin Albumin Creatinine Ratio ≥30 mg/g Crea hos patienter med et Urin Albumin Creatinine Ratio <30 mg/g Crea ved baseline.
|
56 måneder
|
|
ONTARGET. Ny Makroalbuminuri
Tidsramme: 56 måneder
|
ONTARGET.
Nefropati underkategori: Ny makroalbuminuri.
Ny makroalbuminuri er defineret som Urin Albumin Creatinine Ratio ≥300 mg/g Crea hos patienter med et Urin Albumin Creatinine Ratio <300 mg/g Crea ved baseline.
|
56 måneder
|
|
ONTARGET. Kombineret endepunkt for fordobling af serumkreatinin, progression til ESRD, ny mikroalbuminuri eller ny makroalbuminuri
Tidsramme: 56 måneder
|
ONTARGET.
Nefropati underkategori: Kombineret endepunkt for fordobling af serumkreatinin, progression til ESRD, ny mikroalbuminuri eller ny makroalbuminuri
|
56 måneder
|
|
ONTARGET. Normalisering Fra Mikro- eller Makroalbuminuri til Normoalbuminuri
Tidsramme: 56 måneder
|
ONTARGET.
Nefropati underkategori: Normalisering fra mikro- eller makroalbuminuri til normoalbuminuri.
Normalisering fra mikro- eller makroalbuminuri til normoalbuminuri er defineret som UACR <30 mg/g Crea hos patienter med en UACR ≥30 mg/g Crea ved baseline.
|
56 måneder
|
|
ONTARGET. Nydiagnosticeret kongestiv hjertesvigt
Tidsramme: 56 måneder
|
Den igangværende Telmisartan Alene og kombination med Ramipril Global Endpoint-forsøg (ONTARGET).
Tid til den første hændelsesanalyse af endepunktet Nyligt diagnosticeret kongestiv hjerteinsufficiens.
|
56 måneder
|
|
ONTARGET. Kardiovaskulær revaskulariseringsprocedure
Tidsramme: 56 måneder
|
Den igangværende Telmisartan Alene og kombination med Ramipril Global Endpoint-forsøg (ONTARGET).
|
56 måneder
|
|
ONTARGET. Nydiagnosticeret diabetes
Tidsramme: 56 måneder
|
Den igangværende Telmisartan Alene og kombination med Ramipril Global Endpoint-forsøg (ONTARGET).
Tid til den første hændelsesanalyse af endepunktet Nydiagnosticeret diabetes.
Kun beregnet for de patienter uden diabetes ved baseline.
|
56 måneder
|
|
ONTARGET. Kognitiv tilbagegang
Tidsramme: 56 måneder
|
Den igangværende Telmisartan Alene og kombination med Ramipril Global Endpoint-forsøg (ONTARGET).
Tid til første begivenhedsanalyse af endepunktet kognitivt fald, dvs.
Sammenligning af den minimale mentale tilstandsevaluering (MMSE) af patienter ved baseline med den ved 2 år og afslutningen af forsøget.
Et fald i MMSE fra baseline repræsenterer et kognitivt fald.
Dette resultatmål er kun tilgængeligt for de patienter, der havde MMSE ved baseline.
|
56 måneder
|
|
ONTARGET. Ny indtræden af atrieflimren
Tidsramme: 56 måneder
|
Den igangværende Telmisartan Alene og kombination med Ramipril Global Endpoint-forsøg (ONTARGET).
Tid til første hændelsesanalyse af endepunkts ny indtræden af atrieflimren.
|
56 måneder
|
|
TRANSCENDERE. Sammensat endepunkt af kardiovaskulær død, ikke-dødelig myokardieinfarkt og ikke-dødelig slagtilfælde
Tidsramme: 56 måneder
|
Telmisartan Randomized Assessment Study in Angiotension Converting Enzyme Inhibitor intolerante forsøgspersoner med kardiovaskulær sygdom (TRANSCEND).
Tid til første hændelsesanalyse af følgende definerede endepunkter, kardiovaskulær død, ikke-dødelig myokardieinfarkt, ikke-dødelig slagtilfælde og hospitalsindlæggelse for kongestiv hjertesvigt.
|
56 måneder
|
|
TRANSCENDERE. Kardiovaskulær død
Tidsramme: 56 måneder
|
Telmisartan Randomized Assessment Study in Angiotension Converting Enzyme Inhibitor intolerante forsøgspersoner med kardiovaskulær sygdom (TRANSCEND).
Tid til den første hændelsesanalyse af endepunktet kardiovaskulær død.
|
56 måneder
|
|
TRANSCENDERE. Ikke-dødelig myokardieinfarkt
Tidsramme: 56 måneder
|
Telmisartan Randomized Assessment Study in Angiotension Converting Enzyme Inhibitor intolerante forsøgspersoner med kardiovaskulær sygdom (TRANSCEND).
Tid til den første hændelsesanalyse af endepunktet ikke-fatalt myokardieinfarkt.
|
56 måneder
|
|
TRANSCENDERE. Ikke-dødelig slagtilfælde
Tidsramme: 56 måneder
|
Telmisartan Randomized Assessment Study in Angiotension Converting Enzyme Inhibitor intolerante forsøgspersoner med kardiovaskulær sygdom (TRANSCEND).
|
56 måneder
|
|
TRANSCENDERE. Hospitalsindlæggelse for kongestiv hjertesvigt
Tidsramme: 56 måneder
|
Telmisartan Randomized Assessment Study in Angiotension Converting Enzyme Inhibitor intolerante forsøgspersoner med kardiovaskulær sygdom (TRANSCEND).
|
56 måneder
|
|
TRANSCENDERE. Fordobling af serumkreatinin
Tidsramme: 56 måneder
|
TRANSCENDERE.
Nefropati underkategori: fordobling af serumkreatinin
|
56 måneder
|
|
TRANSCENDERE. Progression til ESRD
Tidsramme: 56 måneder
|
TRANSCENDERE.
Nefropati underkategori: Progression til ESRD.
Progression til ESRD er defineret som påbegyndelse af dialyse, behov for nyretransplantation eller eGFR <15 ml/min/1,73m²
|
56 måneder
|
|
TRANSCENDERE. Ny mikroalbuminuri
Tidsramme: 56 måneder
|
TRANSCENDERE.
Nefropati underkategori: Ny mikroalbuminuri.
Ny mikroalbuminuri er defineret som UACR ≥30 mg/g kreatinin [Crea] hos patienter med en UACR <30 mg/g Crea ved baseline
|
56 måneder
|
|
TRANSCENDERE. Ny Makroalbuminuri
Tidsramme: 56 måneder
|
TRANSCENDERE.
Nefropati underkategori: Ny makroalbuminuri.
Ny makroalbuminuri er defineret som UACR ≥300 mg/g kreatinin [Crea] hos patienter med en UACR <300 mg/g Crea ved baseline
|
56 måneder
|
|
TRANSCENDERE. Kombineret endepunkt for fordobling af serumkreatinin, progression til ESRD, ny mikroalbuminuri eller ny makroalbuminuri
Tidsramme: 56 måneder
|
TRANSCENDERE.
Nefropati underkategori: Kombineret endepunkt af fordobling af serumkreatinin, progression til ESRD, ny mikroalbuminuri eller ny makroalbuminuri
|
56 måneder
|
|
TRANSCENDERE. Normalisering Fra Mikro- eller Makroalbuminuri til Normoalbuminuri
Tidsramme: 56 måneder
|
TRANSCENDERE.
Nefropati underkategori: Normalisering fra mikro- eller makroalbuminuri til normoalbuminuri.
Normalisering fra mikro- eller makroalbuminuri til normoalbuminuri er defineret som UACR <30 mg/g Crea hos patienter med en UACR ≥30 mg/g Crea ved baseline.
|
56 måneder
|
|
TRANSCENDERE. Ny indtræden af atrieflimren
Tidsramme: 56 måneder
|
Telmisartan Randomized Assessment Study in Angiotension Converting Enzyme Inhibitor intolerante forsøgspersoner med kardiovaskulær sygdom (TRANSCEND).
|
56 måneder
|
|
TRANSCENDERE. Kognitiv tilbagegang
Tidsramme: 56 måneder
|
Telmisartan Randomized Assessment Study in Angiotension Converting Enzyme Inhibitor intolerante forsøgspersoner med kardiovaskulær sygdom (TRANSCEND).
Tid til første begivenhedsanalyse af endepunktet kognitivt fald, dvs.
Sammenligning af den minimale mentale tilstandsevaluering (MMSE) af patienter ved baseline med den ved 2 år og afslutningen af forsøget.
Et fald i MMSE fra baseline repræsenterer et kognitivt fald.
Dette resultatmål er kun tilgængeligt for de patienter, der havde MMSE ved baseline.
|
56 måneder
|
|
TRANSCENDERE. Nydiagnosticeret diabetes
Tidsramme: 56 måneder
|
Telmisartan Randomized Assessment Study in Angiotension Converting Enzyme Inhibitor intolerante forsøgspersoner med kardiovaskulær sygdom (TRANSCEND).
Tid til den første hændelsesanalyse af endepunktet Nydiagnosticeret diabetes.
Kun beregnet for de patienter uden diabetes ved baseline.
|
56 måneder
|
|
TRANSCENDERE. Kardiovaskulær revaskulariseringsprocedure
Tidsramme: 56 måneder
|
Telmisartan Randomized Assessment Study in Angiotension Converting Enzyme Inhibitor intolerante forsøgspersoner med kardiovaskulær sygdom (TRANSCEND).
|
56 måneder
|
|
TRANSCENDERE. Nydiagnosticeret kongestiv hjertesvigt
Tidsramme: 56 måneder
|
Telmisartan Randomized Assessment Study in Angiotension Converting Enzyme Inhibitor intolerante forsøgspersoner med kardiovaskulær sygdom (TRANSCEND).
|
56 måneder
|
Samarbejdspartnere og efterforskere
Sponsor
Publikationer og nyttige links
Generelle publikationer
- Bohm M, Schumacher H, Werner C, Teo KK, Lonn EM, Mahfoud F, Speer T, Mancia G, Redon J, Schmieder RE, Sliwa K, Marx N, Weber MA, Laufs U, Williams B, Yusuf S, Mann JFE. Association between exercise frequency with renal and cardiovascular outcomes in diabetic and non-diabetic individuals at high cardiovascular risk. Cardiovasc Diabetol. 2022 Jan 20;21(1):12. doi: 10.1186/s12933-021-01429-w.
- Bohm M, Schumacher H, Teo KK, Lonn EM, Lauder L, Mancia G, Redon J, Schmieder RE, Sliwa K, Marx N, Weber MA, Williams B, Yusuf S, Mann JFE, Mahfoud F. Cardiovascular outcomes in patients at high cardiovascular risk with previous myocardial infarction or stroke. J Hypertens. 2021 Aug 1;39(8):1602-1610. doi: 10.1097/HJH.0000000000002822.
- Bohm M, Schumacher H, Teo KK, Lonn EM, Mahfoud F, Emrich I, Mancia G, Redon J, Schmieder RE, Sliwa K, Lehrke M, Marx N, Weber MA, Williams B, Yusuf S, Mann JFE. Renal outcomes and blood pressure patterns in diabetic and nondiabetic individuals at high cardiovascular risk. J Hypertens. 2021 Apr 1;39(4):766-774. doi: 10.1097/HJH.0000000000002697.
- Mancia G, Schumacher H, Bohm M, Mann JFE, Redon J, Facchetti R, Schmieder RE, Lonn EM, Teo KK, Yusuf S. Visit-to-visit blood pressure variability and renal outcomes: results from ONTARGET and TRANSCEND trials. J Hypertens. 2020 Oct;38(10):2050-2058. doi: 10.1097/HJH.0000000000002567.
- Dehghan M, Mente A, Rangarajan S, Mohan V, Lear S, Swaminathan S, Wielgosz A, Seron P, Avezum A, Lopez-Jaramillo P, Turbide G, Chifamba J, AlHabib KF, Mohammadifard N, Szuba A, Khatib R, Altuntas Y, Liu X, Iqbal R, Rosengren A, Yusuf R, Smuts M, Yusufali A, Li N, Diaz R, Yusoff K, Kaur M, Soman B, Ismail N, Gupta R, Dans A, Sheridan P, Teo K, Anand SS, Yusuf S. Association of egg intake with blood lipids, cardiovascular disease, and mortality in 177,000 people in 50 countries. Am J Clin Nutr. 2020 Apr 1;111(4):795-803. doi: 10.1093/ajcn/nqz348.
- Bohm M, Schumacher H, Teo KK, Lonn EM, Mahfoud F, Mann JFE, Mancia G, Redon J, Schmieder RE, Marx N, Sliwa K, Weber MA, Williams B, Yusuf S. Cardiovascular outcomes and achieved blood pressure in patients with and without diabetes at high cardiovascular risk. Eur Heart J. 2019 Jul 1;40(25):2032-2043. doi: 10.1093/eurheartj/ehz149.
- Bohm M, Schumacher H, Teo KK, Lonn EM, Mahfoud F, Ukena C, Mann JFE, Mancia G, Redon J, Schmieder RE, Sliwa K, Marx N, Weber MA, Williams B, Yusuf S. Resting heart rate and cardiovascular outcomes in diabetic and non-diabetic individuals at high cardiovascular risk analysis from the ONTARGET/TRANSCEND trials. Eur Heart J. 2020 Jan 7;41(2):231-238. doi: 10.1093/eurheartj/ehy808.
- Bohm M, Schumacher H, Teo KK, Lonn EM, Mahfoud F, Mann JFE, Mancia G, Redon J, Schmieder RE, Sliwa K, Weber MA, Williams B, Yusuf S. Achieved blood pressure and cardiovascular outcomes in high-risk patients: results from ONTARGET and TRANSCEND trials. Lancet. 2017 Jun 3;389(10085):2226-2237. doi: 10.1016/S0140-6736(17)30754-7. Epub 2017 Apr 5.
- Dunkler D, Kohl M, Teo KK, Heinze G, Dehghan M, Clase CM, Gao P, Yusuf S, Mann JF, Oberbauer R. Dietary risk factors for incidence or progression of chronic kidney disease in individuals with type 2 diabetes in the European Union. Nephrol Dial Transplant. 2015 Aug;30 Suppl 4:iv76-85. doi: 10.1093/ndt/gfv086.
- Bohm M, Schumacher H, Leong D, Mancia G, Unger T, Schmieder R, Custodis F, Diener HC, Laufs U, Lonn E, Sliwa K, Teo K, Fagard R, Redon J, Sleight P, Anderson C, O'Donnell M, Yusuf S. Systolic blood pressure variation and mean heart rate is associated with cognitive dysfunction in patients with high cardiovascular risk. Hypertension. 2015 Mar;65(3):651-61. doi: 10.1161/HYPERTENSIONAHA.114.04568. Epub 2015 Jan 12.
- Verdecchia P, Reboldi G, Angeli F, Trimarco B, Mancia G, Pogue J, Gao P, Sleight P, Teo K, Yusuf S. Systolic and diastolic blood pressure changes in relation with myocardial infarction and stroke in patients with coronary artery disease. Hypertension. 2015 Jan;65(1):108-14. doi: 10.1161/HYPERTENSIONAHA.114.04310. Epub 2014 Oct 20.
- Lonn EM, Rambihar S, Gao P, Custodis FF, Sliwa K, Teo KK, Yusuf S, Bohm M. Heart rate is associated with increased risk of major cardiovascular events, cardiovascular and all-cause death in patients with stable chronic cardiovascular disease: an analysis of ONTARGET/TRANSCEND. Clin Res Cardiol. 2014 Feb;103(2):149-59. doi: 10.1007/s00392-013-0644-4. Epub 2013 Dec 20.
- Heerspink HJ, Gao P, de Zeeuw D, Clase C, Dagenais GR, Sleight P, Lonn E, Teo KT, Yusuf S, Mann JF. The effect of ramipril and telmisartan on serum potassium and its association with cardiovascular and renal events: results from the ONTARGET trial. Eur J Prev Cardiol. 2014 Mar;21(3):299-309. doi: 10.1177/2047487313510678. Epub 2013 Nov 4.
- Dunkler D, Dehghan M, Teo KK, Heinze G, Gao P, Kohl M, Clase CM, Mann JF, Yusuf S, Oberbauer R; ONTARGET Investigators. Diet and kidney disease in high-risk individuals with type 2 diabetes mellitus. JAMA Intern Med. 2013 Oct 14;173(18):1682-92. doi: 10.1001/jamainternmed.2013.9051.
- Bohm M, Schumacher H, Laufs U, Sleight P, Schmieder R, Unger T, Teo K, Yusuf S. Effects of nonpersistence with medication on outcomes in high-risk patients with cardiovascular disease. Am Heart J. 2013 Aug;166(2):306-314.e7. doi: 10.1016/j.ahj.2013.04.016. Epub 2013 Jun 24.
- Dehghan M, Mente A, Teo KK, Gao P, Sleight P, Dagenais G, Avezum A, Probstfield JL, Dans T, Yusuf S; Ongoing Telmisartan Alone and in Combination With Ramipril Global End Point Trial (ONTARGET)/Telmisartan Randomized Assessment Study in ACEI Intolerant Subjects With Cardiovascular Disease (TRANSCEND) Trial Investigators. Relationship between healthy diet and risk of cardiovascular disease among patients on drug therapies for secondary prevention: a prospective cohort study of 31 546 high-risk individuals from 40 countries. Circulation. 2012 Dec 4;126(23):2705-12. doi: 10.1161/CIRCULATIONAHA.112.103234.
- Barzilay JI, Gao P, Clase CM, Mente A, Mann JF, Sleight P, Yusuf S, Teo KK; OnTARGET/TRANSCEND Investigators. Albuminuria and rapid loss of GFR and risk of new hip and pelvic fractures. Clin J Am Soc Nephrol. 2013 Feb;8(2):233-40. doi: 10.2215/CJN.06640712. Epub 2012 Nov 26.
- Kappert K, Bohm M, Schmieder R, Schumacher H, Teo K, Yusuf S, Sleight P, Unger T; ONTARGET/TRANSCEND Investigators. Impact of sex on cardiovascular outcome in patients at high cardiovascular risk: analysis of the Telmisartan Randomized Assessment Study in ACE-Intolerant Subjects With Cardiovascular Disease (TRANSCEND) and the Ongoing Telmisartan Alone and in Combination With Ramipril Global End Point Trial (ONTARGET). Circulation. 2012 Aug 21;126(8):934-41. doi: 10.1161/CIRCULATIONAHA.111.086660. Epub 2012 Jul 24.
- Neumann I, Grassi B. [Critically appraised article]. Rev Med Chil. 2012 Jan;140(1):117-20. Epub 2012 Apr 12. Spanish.
- Verdecchia P, Dagenais G, Healey J, Gao P, Dans AL, Chazova I, Binbrek AS, Iacobellis G, Ferreira R, Holwerda N, Karatzas N, Keltai M, Mancia G, Sleight P, Teo K, Yusuf S; Ongoing Telmisartan Alone and in Combination With Ramipril Global Endpoint TrialTelmisartan Randomized AssessmeNt Study in ACE iNtolerant subjects with cardiovascular Disease Investigators. Blood pressure and other determinants of new-onset atrial fibrillation in patients at high cardiovascular risk in the Ongoing Telmisartan Alone and in Combination With Ramipril Global Endpoint Trial/Telmisartan Randomized AssessmeNt Study in ACE iNtolerant subjects with cardiovascular Disease studies. J Hypertens. 2012 May;30(5):1004-14. doi: 10.1097/HJH.0b013e3283522a51.
- Redon J, Mancia G, Sleight P, Schumacher H, Gao P, Pogue J, Fagard R, Verdecchia P, Weber M, Bohm M, Williams B, Yusoff K, Teo K, Yusuf S; ONTARGET Investigators. Safety and efficacy of low blood pressures among patients with diabetes: subgroup analyses from the ONTARGET (ONgoing Telmisartan Alone and in combination with Ramipril Global Endpoint Trial). J Am Coll Cardiol. 2012 Jan 3;59(1):74-83. doi: 10.1016/j.jacc.2011.09.040.
- Mancia G, Schumacher H, Redon J, Verdecchia P, Schmieder R, Jennings G, Yusoff K, Ryden L, Liu GL, Teo K, Sleight P, Yusuf S. Blood pressure targets recommended by guidelines and incidence of cardiovascular and renal events in the Ongoing Telmisartan Alone and in Combination With Ramipril Global Endpoint Trial (ONTARGET). Circulation. 2011 Oct 18;124(16):1727-36. doi: 10.1161/CIRCULATIONAHA.110.008870. Epub 2011 Sep 26.
- Barzilay JI, Gao P, Ryden L, Schumacher H, Probstfield J, Commerford P, Dans A, Ferreira R, Keltai M, Paolasso E, Yusuf S, Teo K; TRANSCEND Investigators. Effects of telmisartan on glucose levels in people at high risk for cardiovascular disease but free from diabetes: the TRANSCEND study. Diabetes Care. 2011 Sep;34(9):1902-7. doi: 10.2337/dc11-0545. Epub 2011 Jul 25.
- Tobe SW, Clase CM, Gao P, McQueen M, Grosshennig A, Wang X, Teo KK, Yusuf S, Mann JF; ONTARGET and TRANSCEND Investigators. Cardiovascular and renal outcomes with telmisartan, ramipril, or both in people at high renal risk: results from the ONTARGET and TRANSCEND studies. Circulation. 2011 Mar 15;123(10):1098-107. doi: 10.1161/CIRCULATIONAHA.110.964171. Epub 2011 Feb 28.
- Barzilay JI, Gao P, O'Donnell M, Mann JF, Anderson C, Fagard R, Probstfield J, Dagenais GR, Teo K, Yusuf S; ONTARGET and TRANSCEND Investigators. Albuminuria and decline in cognitive function: The ONTARGET/TRANSCEND studies. Arch Intern Med. 2011 Jan 24;171(2):142-50. doi: 10.1001/archinternmed.2010.502.
- Dans AL, Teo K, Gao P, Chen JH, Jae-Hyung K, Yusoff K, Chaithiraphan S, Zhu J, Lisheng L, Yusuf S; Ongoing Telmisartan Alone and in Combination with Ramipril Global Endpoint Trial Investigators. In a subgroup of high-risk Asians, telmisartan was non-inferior to ramipril and better tolerated in the prevention of cardiovascular events. PLoS One. 2010 Dec 21;5(12):e13694. doi: 10.1371/journal.pone.0013694.
- Anderson C, Teo K, Gao P, Arima H, Dans A, Unger T, Commerford P, Dyal L, Schumacher H, Pogue J, Paolasso E, Holwerda N, Chazova I, Binbrek A, Young J, Yusuf S; ONTARGET and TRANSCEND Investigators. Renin-angiotensin system blockade and cognitive function in patients at high risk of cardiovascular disease: analysis of data from the ONTARGET and TRANSCEND studies. Lancet Neurol. 2011 Jan;10(1):43-53. doi: 10.1016/S1474-4422(10)70250-7. Epub 2010 Oct 25.
- Bohm M, Baumhakel M, Teo K, Sleight P, Probstfield J, Gao P, Mann JF, Diaz R, Dagenais GR, Jennings GL, Liu L, Jansky P, Yusuf S; ONTARGET/TRANSCEND Erectile Dysfunction Substudy Investigators. Erectile dysfunction predicts cardiovascular events in high-risk patients receiving telmisartan, ramipril, or both: The ONgoing Telmisartan Alone and in combination with Ramipril Global Endpoint Trial/Telmisartan Randomized AssessmeNt Study in ACE iNtolerant subjects with cardiovascular Disease (ONTARGET/TRANSCEND) Trials. Circulation. 2010 Mar 30;121(12):1439-46. doi: 10.1161/CIRCULATIONAHA.109.864199. Epub 2010 Mar 15.
- Verdecchia P, Sleight P, Mancia G, Fagard R, Trimarco B, Schmieder RE, Kim JH, Jennings G, Jansky P, Chen JH, Liu L, Gao P, Probstfield J, Teo K, Yusuf S; ONTARGET/TRANSCEND Investigators. Effects of telmisartan, ramipril, and their combination on left ventricular hypertrophy in individuals at high vascular risk in the Ongoing Telmisartan Alone and in Combination With Ramipril Global End Point Trial and the Telmisartan Randomized Assessment Study in ACE Intolerant Subjects With Cardiovascular Disease. Circulation. 2009 Oct 6;120(14):1380-9. doi: 10.1161/CIRCULATIONAHA.109.865774. Epub 2009 Sep 21.
- Sleight P, Redon J, Verdecchia P, Mancia G, Gao P, Fagard R, Schumacher H, Weber M, Bohm M, Williams B, Pogue J, Koon T, Yusuf S; ONTARGET investigators. Prognostic value of blood pressure in patients with high vascular risk in the Ongoing Telmisartan Alone and in combination with Ramipril Global Endpoint Trial study. J Hypertens. 2009 Jul;27(7):1360-9. doi: 10.1097/HJH.0b013e32832d7370.
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- Mann JF, Schmieder RE, McQueen M, Dyal L, Schumacher H, Pogue J, Wang X, Maggioni A, Budaj A, Chaithiraphan S, Dickstein K, Keltai M, Metsarinne K, Oto A, Parkhomenko A, Piegas LS, Svendsen TL, Teo KK, Yusuf S; ONTARGET investigators. Renal outcomes with telmisartan, ramipril, or both, in people at high vascular risk (the ONTARGET study): a multicentre, randomised, double-blind, controlled trial. Lancet. 2008 Aug 16;372(9638):547-53. doi: 10.1016/S0140-6736(08)61236-2.
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- Held C, Gerstein HC, Yusuf S, Zhao F, Hilbrich L, Anderson C, Sleight P, Teo K; ONTARGET/TRANSCEND Investigators. Glucose levels predict hospitalization for congestive heart failure in patients at high cardiovascular risk. Circulation. 2007 Mar 20;115(11):1371-5. doi: 10.1161/CIRCULATIONAHA.106.661405. Epub 2007 Mar 5.
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