- ICH GCP
- Register voor klinische proeven in de VS.
- Klinische proef NCT00329238
Secondary Prevention of Venous Thrombo Embolism (VTE). (RE-MEDY)
8 mei 2014 bijgewerkt door: Boehringer Ingelheim
A Phase III, Randomised, Multicenter, Double-blind, Parallel-group, Active Controlled Study to Evaluate the Efficacy and Safety of Oral Dabigatran Etexilate (150 mg Bid) Compared to Warfarin (INR 2.0-3.0) for the Secondary Prevention of Venous Thromboembolism.
The general aim of this study is to determine the comparative safety and efficacy of dabigatran etexilate administered orally and warfarin (International Normalized Ratio (INR) of 2.0-3.0) for the long-term treatment and secondary prevention of symptomatic venous thromboembolism in patients who have been successfully treated with standard doses of an approved anticoagulant for three to twelve months for confirmed acute symptomatic Venous Thrombo-embolism.
Studie Overzicht
Toestand
Voltooid
Conditie
Interventie / Behandeling
Studietype
Ingrijpend
Inschrijving (Werkelijk)
2867
Fase
- Fase 3
Contacten en locaties
In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.
Studie Locaties
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Adrogué, Argentinië
- 1160.47.54017 Boehringer Ingelheim Investigational Site
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Bahía Blanca, Argentinië
- 1160.47.54015 Boehringer Ingelheim Investigational Site
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Capital Federal, Argentinië
- 1160.47.54001 Boehringer Ingelheim Investigational Site
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Capital Federal, Argentinië
- 1160.47.54003 Boehringer Ingelheim Investigational Site
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Capital Federal, Argentinië
- 1160.47.54005 Boehringer Ingelheim Investigational Site
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Capital Federal, Argentinië
- 1160.47.54006 Boehringer Ingelheim Investigational Site
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Capital Federal, Argentinië
- 1160.47.54007 Boehringer Ingelheim Investigational Site
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Capital Federal, Argentinië
- 1160.47.54010 Boehringer Ingelheim Investigational Site
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La Plata, Argentinië
- 1160.47.54016 Boehringer Ingelheim Investigational Site
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Mar del Plata, Argentinië
- 1160.47.54014 Boehringer Ingelheim Investigational Site
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Quilmes, Argentinië
- 1160.47.54013 Boehringer Ingelheim Investigational Site
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Rosario, Argentinië
- 1160.47.54011 Boehringer Ingelheim Investigational Site
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Salta, Argentinië
- 1160.47.54018 Boehringer Ingelheim Investigational Site
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Santa Fe, Argentinië
- 1160.47.54012 Boehringer Ingelheim Investigational Site
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Queensland
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Wooloongabba, Queensland, Australië
- 1160.47.61002 Princess Alexandra Hospital
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South Australia
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Bedford Park, South Australia, Australië
- 1160.47.61004 Boehringer Ingelheim Investigational Site
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Victoria
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Box Hill, Victoria, Australië
- 1160.47.61003 Boehringer Ingelheim Investigational Site
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Clayton, Victoria, Australië
- 1160.47.61001 Boehringer Ingelheim Investigational Site
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Windsor, Victoria, Australië
- 1160.47.61006 Boehringer Ingelheim Investigational Site
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Western Australia
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Perth, Western Australia, Australië
- 1160.47.61005 Boehringer Ingelheim Investigational Site
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Bruxelles, België
- 1160.47.32001 Boehringer Ingelheim Investigational Site
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Bruxelles, België
- 1160.47.32002 Boehringer Ingelheim Investigational Site
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Leuven, België
- 1160.47.32005 Boehringer Ingelheim Investigational Site
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Liège, België
- 1160.47.32004 Boehringer Ingelheim Investigational Site
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Brasília, Brazilië
- 1160.47.55010 Boehringer Ingelheim Investigational Site
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Campinas - SP, Brazilië
- 1160.47.55007 Boehringer Ingelheim Investigational Site
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Curitiba, Brazilië
- 1160.47.55014 Boehringer Ingelheim Investigational Site
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Juvene - Paraná -, Brazilië
- 1160.47.55017 Boehringer Ingelheim Investigational Site
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Rio de Janeiro - RJ, Brazilië
- 1160.47.55016 Boehringer Ingelheim Investigational Site
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São Bernardo do Campo, Brazilië
- 1160.47.55018 Boehringer Ingelheim Investigational Site
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São José do Rio Preto, Brazilië
- 1160.47.55005 Boehringer Ingelheim Investigational Site
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pTO aLEGRE, Brazilië
- 1160.47.55012 Boehringer Ingelheim Investigational Site
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Plovdiv, Bulgarije
- 1160.47.35910 Boehringer Ingelheim Investigational Site
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Rousse, Bulgarije
- 1160.47.35908 Boehringer Ingelheim Investigational Site
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Sofia, Bulgarije
- 1160.47.35901 Boehringer Ingelheim Investigational Site
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Sofia, Bulgarije
- 1160.47.35903 Boehringer Ingelheim Investigational Site
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Sofia, Bulgarije
- 1160.47.35904 Boehringer Ingelheim Investigational Site
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Sofia, Bulgarije
- 1160.47.35906 Boehringer Ingelheim Investigational Site
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Sofia, Bulgarije
- 1160.47.35907 Boehringer Ingelheim Investigational Site
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Varna, Bulgarije
- 1160.47.35905 Boehringer Ingelheim Investigational Site
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Alberta
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Edmonton, Alberta, Canada
- 1160.47.02006 Boehringer Ingelheim Investigational Site
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Edmonton, Alberta, Canada
- 1160.47.02013 Boehringer Ingelheim Investigational Site
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British Columbia
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Victoria, British Columbia, Canada
- 1160.47.02021 Boehringer Ingelheim Investigational Site
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New Brunswick
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Saint Johns, New Brunswick, Canada
- 1160.47.02004 Boehringer Ingelheim Investigational Site
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Nova Scotia
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Halifax, Nova Scotia, Canada
- 1160.47.02001 Boehringer Ingelheim Investigational Site
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Ontario
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Hamilton, Ontario, Canada
- 1160.47.02002 Boehringer Ingelheim Investigational Site
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Hamilton, Ontario, Canada
- 1160.47.02005 Boehringer Ingelheim Investigational Site
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Hamilton, Ontario, Canada
- 1160.47.02010 Boehringer Ingelheim Investigational Site
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Hamilton, Ontario, Canada
- 1160.47.02022 Boehringer Ingelheim Investigational Site
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Ottawa, Ontario, Canada
- 1160.47.02015 Boehringer Ingelheim Investigational Site
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Toronto, Ontario, Canada
- 1160.47.02019 Boehringer Ingelheim Investigational Site
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Quebec
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Montreal, Quebec, Canada
- 1160.47.02008 Boehringer Ingelheim Investigational Site
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Montreal, Quebec, Canada
- 1160.47.02009 Boehringer Ingelheim Investigational Site
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Montreal, Quebec, Canada
- 1160.47.02014 Boehringer Ingelheim Investigational Site
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Montreal, Quebec, Canada
- 1160.47.02017 Boehringer Ingelheim Investigational Site
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Beijing, China
- 1160.47.86001 Boehringer Ingelheim Investigational Site
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Beijing, China
- 1160.47.86015 Boehringer Ingelheim Investigational Site
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Chengdu, China
- 1160.47.86014 Boehringer Ingelheim Investigational Site
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Guangzhou, China
- 1160.47.86012 Boehringer Ingelheim Investigational Site
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Hangzhou, China
- 1160.47.86009 Boehringer Ingelheim Investigational Site
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Hangzhou, China
- 1160.47.86010 Boehringer Ingelheim Investigational Site
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Nanjing, China
- 1160.47.86013 Boehringer Ingelheim Investigational Site
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Shanghai, China
- 1160.47.86002 Boehringer Ingelheim Investigational Site
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Shanghai, China
- 1160.47.86003 Boehringer Ingelheim Investigational Site
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Shanghai, China
- 1160.47.86004 Boehringer Ingelheim Investigational Site
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Shanghai, China
- 1160.47.86005 Boehringer Ingelheim Investigational Site
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Shanghai, China
- 1160.47.86006 Boehringer Ingelheim Investigational Site
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Shanghai, China
- 1160.47.86007 Boehringer Ingelheim Investigational Site
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Shanghai, China
- 1160.47.86016 Boehringer Ingelheim Investigational Site
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Shijiazhuang, China
- 1160.47.86011 Boehringer Ingelheim Investigational Site
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Esbjerg, Denemarken
- 1160.47.45008 Boehringer Ingelheim Investigational Site
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Holbæk, Denemarken
- 1160.47.45009 Boehringer Ingelheim Investigational Site
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Kolding, Denemarken
- 1160.47.45002 Boehringer Ingelheim Investigational Site
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København NV, Denemarken
- 1160.47.45004 Boehringer Ingelheim Investigational Site
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København S, Denemarken
- 1160.47.45007 Boehringer Ingelheim Investigational Site
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Slagelse, Denemarken
- 1160.47.45006 Boehringer Ingelheim Investigational Site
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Dresden, Duitsland
- 1160.47.49017 Boehringer Ingelheim Investigational Site
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Dresden, Duitsland
- 1160.47.49018 Boehringer Ingelheim Investigational Site
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Köln, Duitsland
- 1160.47.49003 Boehringer Ingelheim Investigational Site
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Mannheim, Duitsland
- 1160.47.49005 Boehringer Ingelheim Investigational Site
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Mannheim, Duitsland
- 1160.47.49006 Boehringer Ingelheim Investigational Site
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München, Duitsland
- 1160.47.49007 Boehringer Ingelheim Investigational Site
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München, Duitsland
- 1160.47.49008 Boehringer Ingelheim Investigational Site
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Püttlingen, Duitsland
- 1160.47.49009 Boehringer Ingelheim Investigational Site
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Espoo, Finland
- 1160.47.35804 Boehringer Ingelheim Investigational Site
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Helsinki, Finland
- 1160.47.35801 Boehringer Ingelheim Investigational Site
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Jyväskylä, Finland
- 1160.47.35802 Boehringer Ingelheim Investigational Site
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Kuopio, Finland
- 1160.47.35805 Boehringer Ingelheim Investigational Site
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Tampere, Finland
- 1160.47.35803 Boehringer Ingelheim Investigational Site
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Brest Cedex, Frankrijk
- 1160.47.3301A Boehringer Ingelheim Investigational Site
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Brest Cedex, Frankrijk
- 1160.47.3301B Boehringer Ingelheim Investigational Site
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Brest Cedex, Frankrijk
- 1160.47.3301C Boehringer Ingelheim Investigational Site
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Brest Cedex, Frankrijk
- 1160.47.3301D Boehringer Ingelheim Investigational Site
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Brest Cedex, Frankrijk
- 1160.47.3301E Boehringer Ingelheim Investigational Site
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Brest Cedex, Frankrijk
- 1160.47.3301F Boehringer Ingelheim Investigational Site
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Brest Cedex, Frankrijk
- 1160.47.3301H Boehringer Ingelheim Investigational Site
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Brest Cedex, Frankrijk
- 1160.47.3301I Boehringer Ingelheim Investigational Site
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Lorient, Frankrijk
- 1160.47.3302A Boehringer Ingelheim Investigational Site
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St Etienne Cedex 2, Frankrijk
- 1160.47.3303A Boehringer Ingelheim Investigational Site
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St Etienne Cedex 2, Frankrijk
- 1160.47.3303B Boehringer Ingelheim Investigational Site
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St Etienne Cedex 2, Frankrijk
- 1160.47.3303C Boehringer Ingelheim Investigational Site
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St Etienne Cedex 2, Frankrijk
- 1160.47.3303D Boehringer Ingelheim Investigational Site
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Vandoeuvre les Nancy, Frankrijk
- 1160.47.3308A Boehringer Ingelheim Investigational Site
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Athens, Griekenland
- 1160.47.30001 Boehringer Ingelheim Investigational Site
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Athens, Griekenland
- 1160.47.30006 Boehringer Ingelheim Investigational Site
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Athens, Griekenland
- 1160.47.30007 Boehringer Ingelheim Investigational Site
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Athens, Griekenland
- 1160.47.30009 Boehringer Ingelheim Investigational Site
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Budapest, Hongarije
- 1160.47.36001 Boehringer Ingelheim Investigational Site
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Budapest, Hongarije
- 1160.47.36006 Boehringer Ingelheim Investigational Site
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Budapest, Hongarije
- 1160.47.36007 Boehringer Ingelheim Investigational Site
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Debrecen, Hongarije
- 1160.47.36002 Boehringer Ingelheim Investigational Site
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Gyula, Hongarije
- 1160.47.36012 Boehringer Ingelheim Investigational Site
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Miskolc, Hongarije
- 1160.47.36004 Boehringer Ingelheim Investigational Site
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Pecs, Hongarije
- 1160.47.36003 Boehringer Ingelheim Investigational Site
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Szombathely, Hongarije
- 1160.47.36011 Boehringer Ingelheim Investigational Site
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Székesfehérvár, Hongarije
- 1160.47.36010 Boehringer Ingelheim Investigational Site
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Ahmedabad, Indië
- 1160.47.91002 Boehringer Ingelheim Investigational Site
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Bangalore, Indië
- 1160.47.91011 Boehringer Ingelheim Investigational Site
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Bangalore, Indië
- 1160.47.91015 Boehringer Ingelheim Investigational Site
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Chennai, Indië
- 1160.47.91012 Boehringer Ingelheim Investigational Site
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Chennai, Indië
- 1160.47.91017 Boehringer Ingelheim Investigational Site
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Madurai, Indië
- 1160.47.91009 Boehringer Ingelheim Investigational Site
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Mysore, Indië
- 1160.47.91007 Boehringer Ingelheim Investigational Site
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New Delhi, Indië
- 1160.47.91003 Boehringer Ingelheim Investigational Site
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New Delhi, Indië
- 1160.47.91010 Boehringer Ingelheim Investigational Site
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Pune, Indië
- 1160.47.91001 Boehringer Ingelheim Investigational Site
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Pune, Indië
- 1160.47.91005 Boehringer Ingelheim Investigational Site
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Pune, Indië
- 1160.47.91008 Boehringer Ingelheim Investigational Site
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Trivandrum, Indië
- 1160.47.91014 Boehringer Ingelheim Investigational Site
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Vadodara, Indië
- 1160.47.91004 Boehringer Ingelheim Investigational Site
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new Delhi, Indië
- 1160.47.91006 Boehringer Ingelheim Investigational Site
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Afula, Israël
- 1160.47.97202 Boehringer Ingelheim Investigational Site
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Ashkelon, Israël
- 1160.47.97207 Boehringer Ingelheim Investigational Site
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Haifa, Israël
- 1160.47.97211 Boehringer Ingelheim Investigational Site
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Holon, Israël
- 1160.47.97203 Boehringer Ingelheim Investigational Site
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Kfar Saba, Israël
- 1160.47.97205 Boehringer Ingelheim Investigational Site
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Petach Tikva, Israël
- 1160.47.97206 Boehringer Ingelheim Investigational Site
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Rehovot, Israël
- 1160.47.97208 Boehringer Ingelheim Investigational Site
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Tel Aviv, Israël
- 1160.47.97210 Boehringer Ingelheim Investigational Site
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Tel Hashomer, Israël
- 1160.47.97204 Boehringer Ingelheim Investigational Site
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Zerifin, Israël
- 1160.47.97201 Boehringer Ingelheim Investigational Site
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Bologna, Italië
- 1160.47.39003 Boehringer Ingelheim Investigational Site
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Cremona, Italië
- 1160.47.39004 Boehringer Ingelheim Investigational Site
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Genova, Italië
- 1160.47.39006 Boehringer Ingelheim Investigational Site
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Milano, Italië
- 1160.47.39008 Boehringer Ingelheim Investigational Site
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Reggio Emilia, Italië
- 1160.47.39007 Boehringer Ingelheim Investigational Site
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Udine, Italië
- 1160.47.39009 Boehringer Ingelheim Investigational Site
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Vittorio Veneto, Italië
- 1160.47.39005 Boehringer Ingelheim Investigational Site
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Ankara, Kalkoen
- 1160.47.90003 Boehringer Ingelheim Investigational Site
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Ankara, Kalkoen
- 1160.47.90004 Boehringer Ingelheim Investigational Site
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Ankara, Kalkoen
- 1160.47.90005 Boehringer Ingelheim Investigational Site
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Istanbul, Kalkoen
- 1160.47.90001 Boehringer Ingelheim Investigational Site
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Istanbul, Kalkoen
- 1160.47.90002 Boehringer Ingelheim Investigational Site
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Istanbul, Kalkoen
- 1160.47.90007 Boehringer Ingelheim Investigational Site
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Izmir, Kalkoen
- 1160.47.90006 Boehringer Ingelheim Investigational Site
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Chihuahua, Mexico
- 1160.47.52036 Boehringer Ingelheim Investigational Site
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Culiacan, Mexico
- 1160.47.52039 Boehringer Ingelheim Investigational Site
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Guadalajara, Jal., Mexico
- 1160.47.52030 Boehringer Ingelheim Investigational Site
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Monterrey, Mexico
- 1160.47.52027 Boehringer Ingelheim Investigational Site
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San Luis Potosí, Mexico
- 1160.47.52034 Boehringer Ingelheim Investigational Site
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Amersfoort, Nederland
- 1160.47.31001 Boehringer Ingelheim Investigational Site
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Amsterdam, Nederland
- 1160.47.31006 Boehringer Ingelheim Investigational Site
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Amsterdam, Nederland
- 1160.47.31007 Boehringer Ingelheim Investigational Site
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Den Bosch, Nederland
- 1160.47.31010 Boehringer Ingelheim Investigational Site
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Heerlen, Nederland
- 1160.47.31014 Boehringer Ingelheim Investigational Site
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Maastricht, Nederland
- 1160.47.31005 Boehringer Ingelheim Investigational Site
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Rotterdam, Nederland
- 1160.47.31004 Boehringer Ingelheim Investigational Site
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Rotterdam, Nederland
- 1160.47.31009 Boehringer Ingelheim Investigational Site
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Christchurch, Nieuw-Zeeland
- 1160.47.64004 Boehringer Ingelheim Investigational Site
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Grafton, Nieuw-Zeeland
- 1160.47.64003 Boehringer Ingelheim Investigational Site
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Otahuhu, Nieuw-Zeeland
- 1160.47.64002 Boehringer Ingelheim Investigational Site
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Takapuna Auckland 9, Nieuw-Zeeland
- 1160.47.64001 Boehringer Ingelheim Investigational Site
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Oslo, Noorwegen
- 1160.47.47001 Boehringer Ingelheim Investigational Site
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Oslo, Noorwegen
- 1160.47.47004 Boehringer Ingelheim Investigational Site
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Rud, Noorwegen
- 1160.47.47003 Boehringer Ingelheim Investigational Site
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Trondheim, Noorwegen
- 1160.47.47005 Boehringer Ingelheim Investigational Site
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Kharkov, Oekraïne
- 1160.47.38002 Boehringer Ingelheim Investigational Site
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Kiev, Oekraïne
- 1160.47.38006 Boehringer Ingelheim Investigational Site
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Vinnitsa, Oekraïne
- 1160.47.38005 Boehringer Ingelheim Investigational Site
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Zaporozhye, Oekraïne
- 1160.47.38003 Boehringer Ingelheim Investigational Site
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Graz, Oostenrijk
- 1160.47.43001 Boehringer Ingelheim Investigational Site
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Innsbruck, Oostenrijk
- 1160.47.43003 Boehringer Ingelheim Investigational Site
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Wien, Oostenrijk
- 1160.47.43002 Boehringer Ingelheim Investigational Site
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Wien, Oostenrijk
- 1160.47.43004 Boehringer Ingelheim Investigational Site
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Kielce, Polen
- 1160.47.48004 Boehringer Ingelheim Investigational Site
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Krakow, Polen
- 1160.47.48005 Boehringer Ingelheim Investigational Site
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Krakow, Polen
- 1160.47.48007 Boehringer Ingelheim Investigational Site
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Poznan, Polen
- 1160.47.48003 Boehringer Ingelheim Investigational Site
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Warsaw, Polen
- 1160.47.48006 Boehringer Ingelheim Investigational Site
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Almada, Portugal
- 1160.47.35104 Boehringer Ingelheim Investigational Site
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Coimbra, Portugal
- 1160.47.35109 Boehringer Ingelheim Investigational Site
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Covilhã, Portugal
- 1160.47.35107 Boehringer Ingelheim Investigational Site
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Lisboa, Portugal
- 1160.47.35101 Boehringer Ingelheim Investigational Site
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Lisboa, Portugal
- 1160.47.35102 Boehringer Ingelheim Investigational Site
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Lisboa, Portugal
- 1160.47.35105 Boehringer Ingelheim Investigational Site
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Belgorod, Russische Federatie
- 1160.47.07022 Boehringer Ingelheim Investigational Site
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Chelyabinsk, Russische Federatie
- 1160.47.07011 Boehringer Ingelheim Investigational Site
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Chelyabinsk, Russische Federatie
- 1160.47.07021 Boehringer Ingelheim Investigational Site
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Ekaterinburg, Russische Federatie
- 1160.47.07007 Boehringer Ingelheim Investigational Site
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Krasnodar, Russische Federatie
- 1160.47.07016 Boehringer Ingelheim Investigational Site
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Kursk, Russische Federatie
- 1160.47.07004 Boehringer Ingelheim Investigational Site
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Novosibirsk, Russische Federatie
- 1160.47.07010 Boehringer Ingelheim Investigational Site
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Omsk, Russische Federatie
- 1160.47.07020 Boehringer Ingelheim Investigational Site
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Pskov, Russische Federatie
- 1160.47.07018 Boehringer Ingelheim Investigational Site
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Rostov-na-Donu, Russische Federatie
- 1160.47.07009 Boehringer Ingelheim Investigational Site
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Rostov-na-Donu, Russische Federatie
- 1160.47.07023 Boehringer Ingelheim Investigational Site
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Rostov-na-Donu, Russische Federatie
- 1160.47.07024 Boehringer Ingelheim Investigational Site
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Rostov-na-Donu, Russische Federatie
- 1160.47.07025 Boehringer Ingelheim Investigational Site
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St. Petersburg, Russische Federatie
- 1160.47.07001 Boehringer Ingelheim Investigational Site
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St. Petersburg, Russische Federatie
- 1160.47.07002 Boehringer Ingelheim Investigational Site
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St. Petersburg, Russische Federatie
- 1160.47.07017 Boehringer Ingelheim Investigational Site
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Tyumen, Russische Federatie
- 1160.47.07019 Boehringer Ingelheim Investigational Site
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Ufa, Russische Federatie
- 1160.47.07014 Boehringer Ingelheim Investigational Site
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Yaroslavl, Russische Federatie
- 1160.47.07005 Boehringer Ingelheim Investigational Site
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Yaroslavl, Russische Federatie
- 1160.47.07006 Boehringer Ingelheim Investigational Site
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Banska Bystrica, Slowakije
- 1160.47.42107 Boehringer Ingelheim Investigational Site
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Lucenec, Slowakije
- 1160.47.42106 Boehringer Ingelheim Investigational Site
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Nitra, Slowakije
- 1160.47.42102 Boehringer Ingelheim Investigational Site
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Nove Zamky, Slowakije
- 1160.47.42103 Boehringer Ingelheim Investigational Site
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Zilina, Slowakije
- 1160.47.42104 Boehringer Ingelheim Investigational Site
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Alicante, Spanje
- 1160.47.34006 Boehringer Ingelheim Investigational Site
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Badalona (Barcelona), Spanje
- 1160.47.34012 Boehringer Ingelheim Investigational Site
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Barcelona, Spanje
- 1160.47.34001 Boehringer Ingelheim Investigational Site
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Barcelona, Spanje
- 1160.47.34002 Boehringer Ingelheim Investigational Site
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Cartagena. Murcia, Spanje
- 1160.47.34007 Boehringer Ingelheim Investigational Site
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Cuenca, Spanje
- 1160.47.34003 Boehringer Ingelheim Investigational Site
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Madrid, Spanje
- 1160.47.34009 Boehringer Ingelheim Investigational Site
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Santander, Spanje
- 1160.47.34004 Boehringer Ingelheim Investigational Site
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Valencia, Spanje
- 1160.47.34011 Boehringer Ingelheim Investigational Site
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Brno, Tsjechische Republiek
- 1160.47.42001 Boehringer Ingelheim Investigational Site
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Hradec Kralove, Tsjechische Republiek
- 1160.47.42002 Boehringer Ingelheim Investigational Site
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Hranice, Tsjechische Republiek
- 1160.47.42011 Boehringer Ingelheim Investigational Site
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Liberec, Tsjechische Republiek
- 1160.47.42012 Boehringer Ingelheim Investigational Site
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Novy Jicin, Tsjechische Republiek
- 1160.47.42015 Boehringer Ingelheim Investigational Site
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Ostrava-Vitkovice, Tsjechische Republiek
- 1160.47.42005 Boehringer Ingelheim Investigational Site
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Praha 2, Tsjechische Republiek
- 1160.47.42004 Boehringer Ingelheim Investigational Site
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Tabor, Tsjechische Republiek
- 1160.47.42014 Boehringer Ingelheim Investigational Site
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Usti nad Labem, Tsjechische Republiek
- 1160.47.42010 Boehringer Ingelheim Investigational Site
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Zlin, Tsjechische Republiek
- 1160.47.42007 Boehringer Ingelheim Investigational Site
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Headington, Oxford, Verenigd Koninkrijk
- 1160.47.44005 Boehringer Ingelheim Investigational Site
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London, Verenigd Koninkrijk
- 1160.47.44009 Boehringer Ingelheim Investigational Site
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London, Verenigd Koninkrijk
- 1160.47.44011 Boehringer Ingelheim Investigational Site
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Newcastle upon Tyne, Verenigd Koninkrijk
- 1160.47.44006 Boehringer Ingelheim Investigational Site
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Sheffield, Verenigd Koninkrijk
- 1160.47.44012 Boehringer Ingelheim Investigational Site
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Alabama
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Mobile, Alabama, Verenigde Staten
- 1160.47.01035 Boehringer Ingelheim Investigational Site
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Connecticut
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Hartford, Connecticut, Verenigde Staten
- 1160.47.01056 Boehringer Ingelheim Investigational Site
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Florida
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Clearwater, Florida, Verenigde Staten
- 1160.47.01044 Boehringer Ingelheim Investigational Site
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Georgia
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Augusta, Georgia, Verenigde Staten
- 1160.47.01019 Boehringer Ingelheim Investigational Site
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Decatur, Georgia, Verenigde Staten
- 1160.47.01008 Boehringer Ingelheim Investigational Site
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Maryland
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Baltimore, Maryland, Verenigde Staten
- 1160.47.01014 Boehringer Ingelheim Investigational Site
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Massachusetts
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Roxbury Crossing, Massachusetts, Verenigde Staten
- 1160.47.01018 Boehringer Ingelheim Investigational Site
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Michigan
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Detroit, Michigan, Verenigde Staten
- 1160.47.01023 Boehringer Ingelheim Investigational Site
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Minnesota
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St. Louis Park, Minnesota, Verenigde Staten
- 1160.47.01009 Boehringer Ingelheim Investigational Site
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New Hampshire
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Lebanon, New Hampshire, Verenigde Staten
- 1160.47.01031 Boehringer Ingelheim Investigational Site
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New Mexico
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Albuquerque, New Mexico, Verenigde Staten
- 1160.47.01036 Boehringer Ingelheim Investigational Site
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North Carolina
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Chapel Hill, North Carolina, Verenigde Staten
- 1160.47.01027 Boehringer Ingelheim Investigational Site
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Winston-Salem, North Carolina, Verenigde Staten
- 1160.47.01039 Boehringer Ingelheim Investigational Site
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North Dakota
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Grand Forks, North Dakota, Verenigde Staten
- 1160.47.01030 Boehringer Ingelheim Investigational Site
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Ohio
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Toledo, Ohio, Verenigde Staten
- 1160.47.01013 Boehringer Ingelheim Investigational Site
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Pennsylvania
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Altoona, Pennsylvania, Verenigde Staten
- 1160.47.01052 Boehringer Ingelheim Investigational Site
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South Carolina
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Summerville, South Carolina, Verenigde Staten
- 1160.47.01055 Boehringer Ingelheim Investigational Site
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Virginia
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Richmond, Virginia, Verenigde Staten
- 1160.47.01017 Boehringer Ingelheim Investigational Site
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Johannesburg, Zuid-Afrika
- 1160.47.27001 Boehringer Ingelheim Investigational Site
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Johannesburg, Zuid-Afrika
- 1160.47.27002 Boehringer Ingelheim Investigational Site
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Johannesburg, Zuid-Afrika
- 1160.47.27006 Boehringer Ingelheim Investigational Site
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Pretoria, Zuid-Afrika
- 1160.47.27007
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Randburg, Zuid-Afrika
- 1160.47.27003 Boehringer Ingelheim Investigational Site
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Roodepoort, Zuid-Afrika
- 1160.47.27005 Boehringer Ingelheim Investigational Site
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Göteborg, Zweden
- 1160.47.46002 Boehringer Ingelheim Investigational Site
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Jönköping, Zweden
- 1160.47.46006 Boehringer Ingelheim Investigational Site
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Stockholm, Zweden
- 1160.47.46001 Boehringer Ingelheim Investigational Site
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Stockholm, Zweden
- 1160.47.46007 Boehringer Ingelheim Investigational Site
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Stockholm, Zweden
- 1160.47.46008 Boehringer Ingelheim Investigational Site
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Sundsvall, Zweden
- 1160.47.46005 Boehringer Ingelheim Investigational Site
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Uppsala, Zweden
- 1160.47.46003 Boehringer Ingelheim Investigational Site
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Deelname Criteria
Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
18 jaar en ouder (Volwassen, Oudere volwassene)
Accepteert gezonde vrijwilligers
Nee
Geslachten die in aanmerking komen voor studie
Allemaal
Beschrijving
Inclusion criteria:
Inclusion_Criteria
- Acute symptomatic deep vein thrombosis (DVT)
- Pulmonary embolism (PE) 3-12 months prior to screening, which has been documented by objective testing
Exclusion criteria:
Exclusion_Criteria
- Symptomatic DVT or PE at screening Interruption of anticoagulant therapy for 2 or more weeks during the 3-12 months of treatment for the prior VTE.
- Patients who in the investigators judgement are perceived as having an excessive risk of bleeding Elevated Aspartate aminotransferase (AST) or Alanine tranminase (ALT) > 2x ULN
- Severe renal impairment (estimated creatinine clearance <= 30 ml/min)
Studie plan
Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Behandeling
- Toewijzing: Gerandomiseerd
- Interventioneel model: Parallelle opdracht
- Masker: Dubbele
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
|---|---|
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Experimenteel: Dabigatran
Patient to receive 1 capsule containing dabigatran 150 mg twice daily plus placebo tablets for warfarin as decided by sham INR measurements
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Dabigatran 150 mg BID (twice daily)
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Actieve vergelijker: Warfarin (INR of 2.0-3.0)
Patient to receive warfarin tablets to target INR 2.0-3.0 plus placebo capsules for dabigatran twice daily
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Warfarin dosed individually to maintain INR 2.0-3.0
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Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
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Composite of Recurrent VTE or VTE Death at 36 Months
Tijdsspanne: 36 months
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Endpoint is a composite of recurrent Venous Thromboembolic Event (VTE) and death related to VTE.
VTE was defined as the composite of symptomatic Deep Vein Thrombosis (DVT) of the leg and Pulmonary embolism (PE).
All recurrent VTEs required objective verification by definitive diagnostic evaluation.
In case of death, autopsy was an additional way to confirm VTE.
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36 months
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Composite of Recurrent VTE or VTE Death at 18 Months
Tijdsspanne: 18 months
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Endpoint is a composite of recurrent Venous Thromboembolic Event (VTE) and death related to VTE.
VTE was defined as the composite of symptomatic Deep Vein Thrombosis (DVT) of the leg and Pulmonary embolism (PE).
All recurrent VTEs required objective verification by definitive diagnostic evaluation.
In case of death, autopsy was an additional way to confirm VTE.
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18 months
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Secundaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
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Composite of Recurrent VTE or All Cause Death at 36 Months
Tijdsspanne: 36 months
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Endpoint is a composite of recurrent Venous Thromboembolic Event (VTE) and all cause death.
VTE was defined as the composite of symptomatic Deep Vein Thrombosis (DVT) of the leg and Pulmonary embolism (PE).
All recurrent VTEs required objective verification by definitive diagnostic evaluation.
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36 months
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Composite of Recurrent VTE or All Cause Death at 18 Months
Tijdsspanne: 18 months
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Endpoint is a composite of recurrent Venous Thromboembolic Event (VTE) and all cause death.
VTE was defined as the composite of symptomatic Deep Vein Thrombosis (DVT) of the leg and Pulmonary embolism (PE).
All recurrent VTEs required objective verification by definitive diagnostic evaluation.
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18 months
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Deep Vein Thrombosis (DVT) at 36 Months
Tijdsspanne: 36 months
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Symptomatic Deep vein thrombosis (DVT).
All DVT events required objective verification through definitive diagnostic evaluation.
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36 months
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DVT at 18 Months
Tijdsspanne: 18 months
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Symptomatic Deep vein thrombosis (DVT).
All DVT events required objective verification through definitive diagnostic evaluation.
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18 months
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Symptomatic Pulmonary Embolism (PE) at 36 Months
Tijdsspanne: 36 months
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Symptomatic pulmonary embolism (PE) at 36 Months (fatal or non-fatal).
All suspected PEs required confirmation by one of the following: ventilation-perfusion (V-Q) lung scan, pulmonary angiography, or spiral (helical) Computed tomography.
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36 months
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Symptomatic Pulmonary Embolism (PE) at 18 Months
Tijdsspanne: 18 months
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Symptomatic pulmonary embolism (PE) at 18 Months (fatal or non-fatal).
All suspected PEs required confirmation by one of the following: ventilation-perfusion (V-Q) lung scan, pulmonary angiography, or spiral (helical) Computed tomography.
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18 months
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Deaths Related to VTE at 36 Months
Tijdsspanne: 36 months
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Deaths related to VTE (i.e.
fatal PE) at 36 Months.
Deaths related to VTE (i.e.
fatal PE) at 18 Months.
All deaths were centrally adjudicated by the Independent Central Adjudication Committee for VTE and death in a treatment-blinded way.
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36 months
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Deaths Related to VTE at 18 Months
Tijdsspanne: 18 months
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Deaths related to VTE (i.e.
fatal PE) at 18 Months.
All deaths were centrally adjudicated by the Independent Central Adjudication Committee for VTE and death in a treatment-blinded way.
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18 months
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Deaths of All Causes at 36 Months
Tijdsspanne: 36 months
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Deaths of all causes at 36 Months.
All components of the primary efficacy endpoint and all deaths were centrally adjudicated by the Independent Central Adjudication Committee for VTE and death without knowledge of any individual treatment assignments.
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36 months
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Deaths of All Causes at 18 Months
Tijdsspanne: 18 months
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Deaths of all causes at 18 Months.
All components of the primary efficacy endpoint and all deaths were centrally adjudicated by the Independent Central Adjudication Committee for VTE and death without knowledge of any individual treatment assignments.
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18 months
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Number of Participants With Bleeding Events
Tijdsspanne: first intake of study drug until 6 days following last intake of study drug
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MBE (major bleeding event) if it fulfilled at least one of the following criteria
Minor bleeding event was any bleeding that did not fulfil any of the criteria for MBEs CRBE (clinically relevant bleeding event) if it is a minor bleeding events which fulfilled at least one of the following criteria
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first intake of study drug until 6 days following last intake of study drug
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Laboratory Analysis
Tijdsspanne: 18 months + 30 days follow up
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Patients with LFT (liver function tests) increases of possible clinical significance during treatment.
Increases of possible clinical significance were defined as: ≥3 x ULN (AST, ALT), ≥2 x ULN (AP), and ≥2 mg/dL (total bilirubin).
Only patients with a baseline value which was not of possible clinical significance (or without any baseline value) could have a PCSA (Possible clinically significant abnormality).
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18 months + 30 days follow up
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Number of Participants With Definite Acute Coronary Syndrome (ACS)
Tijdsspanne: day of first study drug intake until last day of study drug intake; from the day after last intake of study drug until trial termination
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All suspected ACS occurring during the trial were to be recorded on the CRF and were to be centrally adjudicated by an independent ACS/AC in a treatment-blinded manner.
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day of first study drug intake until last day of study drug intake; from the day after last intake of study drug until trial termination
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Medewerkers en onderzoekers
Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.
Sponsor
Publicaties en nuttige links
De persoon die verantwoordelijk is voor het invoeren van informatie over het onderzoek stelt deze publicaties vrijwillig ter beschikking. Dit kan gaan over alles wat met het onderzoek te maken heeft.
Algemene publicaties
- Majeed A, Hwang HG, Connolly SJ, Eikelboom JW, Ezekowitz MD, Wallentin L, Brueckmann M, Fraessdorf M, Yusuf S, Schulman S. Management and outcomes of major bleeding during treatment with dabigatran or warfarin. Circulation. 2013 Nov 19;128(21):2325-32. doi: 10.1161/CIRCULATIONAHA.113.002332. Epub 2013 Sep 30.
- Goldhaber SZ, Eriksson H, Kakkar A, Schellong S, Feuring M, Fraessdorf M, Kreuzer J, Schueler E, Schulman S. Efficacy of dabigatran versus warfarin in patients with acute venous thromboembolism in the presence of thrombophilia: Findings from RE-COVER(R), RE-COVER II, and RE-MEDY. Vasc Med. 2016 Dec;21(6):506-514. doi: 10.1177/1358863X16668588. Epub 2016 Nov 1.
- Schulman S, Kearon C, Kakkar AK, Schellong S, Eriksson H, Baanstra D, Kvamme AM, Friedman J, Mismetti P, Goldhaber SZ; RE-MEDY Trial Investigators; RE-SONATE Trial Investigators. Extended use of dabigatran, warfarin, or placebo in venous thromboembolism. N Engl J Med. 2013 Feb 21;368(8):709-18. doi: 10.1056/NEJMoa1113697.
Nuttige links
Studie record data
Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.
Bestudeer belangrijke data
Studie start
1 mei 2006
Primaire voltooiing (Werkelijk)
1 oktober 2010
Studieregistratiedata
Eerst ingediend
23 mei 2006
Eerst ingediend dat voldeed aan de QC-criteria
23 mei 2006
Eerst geplaatst (Schatting)
24 mei 2006
Updates van studierecords
Laatste update geplaatst (Schatting)
19 mei 2014
Laatste update ingediend die voldeed aan QC-criteria
8 mei 2014
Laatst geverifieerd
1 december 2013
Meer informatie
Termen gerelateerd aan deze studie
Aanvullende relevante MeSH-voorwaarden
Andere studie-ID-nummers
- 1160.47
- 2005-002536-94 (EudraCT-nummer: EudraCT)
Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .