- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT00329238
Secondary Prevention of Venous Thrombo Embolism (VTE). (RE-MEDY)
8 de mayo de 2014 actualizado por: 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.
Descripción general del estudio
Estado
Terminado
Condiciones
Intervención / Tratamiento
Tipo de estudio
Intervencionista
Inscripción (Actual)
2867
Fase
- Fase 3
Contactos y Ubicaciones
Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.
Ubicaciones de estudio
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Dresden, Alemania
- 1160.47.49017 Boehringer Ingelheim Investigational Site
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Dresden, Alemania
- 1160.47.49018 Boehringer Ingelheim Investigational Site
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Köln, Alemania
- 1160.47.49003 Boehringer Ingelheim Investigational Site
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Mannheim, Alemania
- 1160.47.49005 Boehringer Ingelheim Investigational Site
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Mannheim, Alemania
- 1160.47.49006 Boehringer Ingelheim Investigational Site
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München, Alemania
- 1160.47.49007 Boehringer Ingelheim Investigational Site
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München, Alemania
- 1160.47.49008 Boehringer Ingelheim Investigational Site
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Püttlingen, Alemania
- 1160.47.49009 Boehringer Ingelheim Investigational Site
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Adrogué, Argentina
- 1160.47.54017 Boehringer Ingelheim Investigational Site
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Bahía Blanca, Argentina
- 1160.47.54015 Boehringer Ingelheim Investigational Site
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Capital Federal, Argentina
- 1160.47.54001 Boehringer Ingelheim Investigational Site
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Capital Federal, Argentina
- 1160.47.54003 Boehringer Ingelheim Investigational Site
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Capital Federal, Argentina
- 1160.47.54005 Boehringer Ingelheim Investigational Site
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Capital Federal, Argentina
- 1160.47.54006 Boehringer Ingelheim Investigational Site
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Capital Federal, Argentina
- 1160.47.54007 Boehringer Ingelheim Investigational Site
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Capital Federal, Argentina
- 1160.47.54010 Boehringer Ingelheim Investigational Site
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La Plata, Argentina
- 1160.47.54016 Boehringer Ingelheim Investigational Site
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Mar del Plata, Argentina
- 1160.47.54014 Boehringer Ingelheim Investigational Site
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Quilmes, Argentina
- 1160.47.54013 Boehringer Ingelheim Investigational Site
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Rosario, Argentina
- 1160.47.54011 Boehringer Ingelheim Investigational Site
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Salta, Argentina
- 1160.47.54018 Boehringer Ingelheim Investigational Site
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Santa Fe, Argentina
- 1160.47.54012 Boehringer Ingelheim Investigational Site
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Queensland
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Wooloongabba, Queensland, Australia
- 1160.47.61002 Princess Alexandra Hospital
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South Australia
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Bedford Park, South Australia, Australia
- 1160.47.61004 Boehringer Ingelheim Investigational Site
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Victoria
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Box Hill, Victoria, Australia
- 1160.47.61003 Boehringer Ingelheim Investigational Site
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Clayton, Victoria, Australia
- 1160.47.61001 Boehringer Ingelheim Investigational Site
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Windsor, Victoria, Australia
- 1160.47.61006 Boehringer Ingelheim Investigational Site
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Western Australia
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Perth, Western Australia, Australia
- 1160.47.61005 Boehringer Ingelheim Investigational Site
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Graz, Austria
- 1160.47.43001 Boehringer Ingelheim Investigational Site
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Innsbruck, Austria
- 1160.47.43003 Boehringer Ingelheim Investigational Site
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Wien, Austria
- 1160.47.43002 Boehringer Ingelheim Investigational Site
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Wien, Austria
- 1160.47.43004 Boehringer Ingelheim Investigational Site
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Brasília, Brasil
- 1160.47.55010 Boehringer Ingelheim Investigational Site
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Campinas - SP, Brasil
- 1160.47.55007 Boehringer Ingelheim Investigational Site
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Curitiba, Brasil
- 1160.47.55014 Boehringer Ingelheim Investigational Site
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Juvene - Paraná -, Brasil
- 1160.47.55017 Boehringer Ingelheim Investigational Site
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Rio de Janeiro - RJ, Brasil
- 1160.47.55016 Boehringer Ingelheim Investigational Site
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São Bernardo do Campo, Brasil
- 1160.47.55018 Boehringer Ingelheim Investigational Site
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São José do Rio Preto, Brasil
- 1160.47.55005 Boehringer Ingelheim Investigational Site
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pTO aLEGRE, Brasil
- 1160.47.55012 Boehringer Ingelheim Investigational Site
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Plovdiv, Bulgaria
- 1160.47.35910 Boehringer Ingelheim Investigational Site
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Rousse, Bulgaria
- 1160.47.35908 Boehringer Ingelheim Investigational Site
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Sofia, Bulgaria
- 1160.47.35901 Boehringer Ingelheim Investigational Site
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Sofia, Bulgaria
- 1160.47.35903 Boehringer Ingelheim Investigational Site
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Sofia, Bulgaria
- 1160.47.35904 Boehringer Ingelheim Investigational Site
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Sofia, Bulgaria
- 1160.47.35906 Boehringer Ingelheim Investigational Site
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Sofia, Bulgaria
- 1160.47.35907 Boehringer Ingelheim Investigational Site
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Varna, Bulgaria
- 1160.47.35905 Boehringer Ingelheim Investigational Site
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Bruxelles, Bélgica
- 1160.47.32001 Boehringer Ingelheim Investigational Site
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Bruxelles, Bélgica
- 1160.47.32002 Boehringer Ingelheim Investigational Site
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Leuven, Bélgica
- 1160.47.32005 Boehringer Ingelheim Investigational Site
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Liège, Bélgica
- 1160.47.32004 Boehringer Ingelheim Investigational Site
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Alberta
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Edmonton, Alberta, Canadá
- 1160.47.02006 Boehringer Ingelheim Investigational Site
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Edmonton, Alberta, Canadá
- 1160.47.02013 Boehringer Ingelheim Investigational Site
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British Columbia
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Victoria, British Columbia, Canadá
- 1160.47.02021 Boehringer Ingelheim Investigational Site
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New Brunswick
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Saint Johns, New Brunswick, Canadá
- 1160.47.02004 Boehringer Ingelheim Investigational Site
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Nova Scotia
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Halifax, Nova Scotia, Canadá
- 1160.47.02001 Boehringer Ingelheim Investigational Site
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Ontario
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Hamilton, Ontario, Canadá
- 1160.47.02002 Boehringer Ingelheim Investigational Site
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Hamilton, Ontario, Canadá
- 1160.47.02005 Boehringer Ingelheim Investigational Site
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Hamilton, Ontario, Canadá
- 1160.47.02010 Boehringer Ingelheim Investigational Site
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Hamilton, Ontario, Canadá
- 1160.47.02022 Boehringer Ingelheim Investigational Site
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Ottawa, Ontario, Canadá
- 1160.47.02015 Boehringer Ingelheim Investigational Site
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Toronto, Ontario, Canadá
- 1160.47.02019 Boehringer Ingelheim Investigational Site
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Quebec
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Montreal, Quebec, Canadá
- 1160.47.02008 Boehringer Ingelheim Investigational Site
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Montreal, Quebec, Canadá
- 1160.47.02009 Boehringer Ingelheim Investigational Site
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Montreal, Quebec, Canadá
- 1160.47.02014 Boehringer Ingelheim Investigational Site
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Montreal, Quebec, Canadá
- 1160.47.02017 Boehringer Ingelheim Investigational Site
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Esbjerg, Dinamarca
- 1160.47.45008 Boehringer Ingelheim Investigational Site
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Holbæk, Dinamarca
- 1160.47.45009 Boehringer Ingelheim Investigational Site
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Kolding, Dinamarca
- 1160.47.45002 Boehringer Ingelheim Investigational Site
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København NV, Dinamarca
- 1160.47.45004 Boehringer Ingelheim Investigational Site
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København S, Dinamarca
- 1160.47.45007 Boehringer Ingelheim Investigational Site
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Slagelse, Dinamarca
- 1160.47.45006 Boehringer Ingelheim Investigational Site
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Banska Bystrica, Eslovaquia
- 1160.47.42107 Boehringer Ingelheim Investigational Site
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Lucenec, Eslovaquia
- 1160.47.42106 Boehringer Ingelheim Investigational Site
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Nitra, Eslovaquia
- 1160.47.42102 Boehringer Ingelheim Investigational Site
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Nove Zamky, Eslovaquia
- 1160.47.42103 Boehringer Ingelheim Investigational Site
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Zilina, Eslovaquia
- 1160.47.42104 Boehringer Ingelheim Investigational Site
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Alicante, España
- 1160.47.34006 Boehringer Ingelheim Investigational Site
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Badalona (Barcelona), España
- 1160.47.34012 Boehringer Ingelheim Investigational Site
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Barcelona, España
- 1160.47.34001 Boehringer Ingelheim Investigational Site
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Barcelona, España
- 1160.47.34002 Boehringer Ingelheim Investigational Site
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Cartagena. Murcia, España
- 1160.47.34007 Boehringer Ingelheim Investigational Site
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Cuenca, España
- 1160.47.34003 Boehringer Ingelheim Investigational Site
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Madrid, España
- 1160.47.34009 Boehringer Ingelheim Investigational Site
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Santander, España
- 1160.47.34004 Boehringer Ingelheim Investigational Site
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Valencia, España
- 1160.47.34011 Boehringer Ingelheim Investigational Site
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Alabama
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Mobile, Alabama, Estados Unidos
- 1160.47.01035 Boehringer Ingelheim Investigational Site
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Connecticut
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Hartford, Connecticut, Estados Unidos
- 1160.47.01056 Boehringer Ingelheim Investigational Site
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Florida
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Clearwater, Florida, Estados Unidos
- 1160.47.01044 Boehringer Ingelheim Investigational Site
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Georgia
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Augusta, Georgia, Estados Unidos
- 1160.47.01019 Boehringer Ingelheim Investigational Site
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Decatur, Georgia, Estados Unidos
- 1160.47.01008 Boehringer Ingelheim Investigational Site
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Maryland
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Baltimore, Maryland, Estados Unidos
- 1160.47.01014 Boehringer Ingelheim Investigational Site
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Massachusetts
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Roxbury Crossing, Massachusetts, Estados Unidos
- 1160.47.01018 Boehringer Ingelheim Investigational Site
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Michigan
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Detroit, Michigan, Estados Unidos
- 1160.47.01023 Boehringer Ingelheim Investigational Site
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Minnesota
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St. Louis Park, Minnesota, Estados Unidos
- 1160.47.01009 Boehringer Ingelheim Investigational Site
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New Hampshire
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Lebanon, New Hampshire, Estados Unidos
- 1160.47.01031 Boehringer Ingelheim Investigational Site
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New Mexico
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Albuquerque, New Mexico, Estados Unidos
- 1160.47.01036 Boehringer Ingelheim Investigational Site
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North Carolina
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Chapel Hill, North Carolina, Estados Unidos
- 1160.47.01027 Boehringer Ingelheim Investigational Site
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Winston-Salem, North Carolina, Estados Unidos
- 1160.47.01039 Boehringer Ingelheim Investigational Site
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North Dakota
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Grand Forks, North Dakota, Estados Unidos
- 1160.47.01030 Boehringer Ingelheim Investigational Site
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Ohio
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Toledo, Ohio, Estados Unidos
- 1160.47.01013 Boehringer Ingelheim Investigational Site
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Pennsylvania
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Altoona, Pennsylvania, Estados Unidos
- 1160.47.01052 Boehringer Ingelheim Investigational Site
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South Carolina
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Summerville, South Carolina, Estados Unidos
- 1160.47.01055 Boehringer Ingelheim Investigational Site
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Virginia
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Richmond, Virginia, Estados Unidos
- 1160.47.01017 Boehringer Ingelheim Investigational Site
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Belgorod, Federación Rusa
- 1160.47.07022 Boehringer Ingelheim Investigational Site
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Chelyabinsk, Federación Rusa
- 1160.47.07011 Boehringer Ingelheim Investigational Site
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Chelyabinsk, Federación Rusa
- 1160.47.07021 Boehringer Ingelheim Investigational Site
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Ekaterinburg, Federación Rusa
- 1160.47.07007 Boehringer Ingelheim Investigational Site
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Krasnodar, Federación Rusa
- 1160.47.07016 Boehringer Ingelheim Investigational Site
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Kursk, Federación Rusa
- 1160.47.07004 Boehringer Ingelheim Investigational Site
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Novosibirsk, Federación Rusa
- 1160.47.07010 Boehringer Ingelheim Investigational Site
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Omsk, Federación Rusa
- 1160.47.07020 Boehringer Ingelheim Investigational Site
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Pskov, Federación Rusa
- 1160.47.07018 Boehringer Ingelheim Investigational Site
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Rostov-na-Donu, Federación Rusa
- 1160.47.07009 Boehringer Ingelheim Investigational Site
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Rostov-na-Donu, Federación Rusa
- 1160.47.07023 Boehringer Ingelheim Investigational Site
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Rostov-na-Donu, Federación Rusa
- 1160.47.07024 Boehringer Ingelheim Investigational Site
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Rostov-na-Donu, Federación Rusa
- 1160.47.07025 Boehringer Ingelheim Investigational Site
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St. Petersburg, Federación Rusa
- 1160.47.07001 Boehringer Ingelheim Investigational Site
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St. Petersburg, Federación Rusa
- 1160.47.07002 Boehringer Ingelheim Investigational Site
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St. Petersburg, Federación Rusa
- 1160.47.07017 Boehringer Ingelheim Investigational Site
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Tyumen, Federación Rusa
- 1160.47.07019 Boehringer Ingelheim Investigational Site
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Ufa, Federación Rusa
- 1160.47.07014 Boehringer Ingelheim Investigational Site
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Yaroslavl, Federación Rusa
- 1160.47.07005 Boehringer Ingelheim Investigational Site
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Yaroslavl, Federación Rusa
- 1160.47.07006 Boehringer Ingelheim Investigational Site
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Espoo, Finlandia
- 1160.47.35804 Boehringer Ingelheim Investigational Site
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Helsinki, Finlandia
- 1160.47.35801 Boehringer Ingelheim Investigational Site
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Jyväskylä, Finlandia
- 1160.47.35802 Boehringer Ingelheim Investigational Site
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Kuopio, Finlandia
- 1160.47.35805 Boehringer Ingelheim Investigational Site
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Tampere, Finlandia
- 1160.47.35803 Boehringer Ingelheim Investigational Site
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Brest Cedex, Francia
- 1160.47.3301A Boehringer Ingelheim Investigational Site
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Brest Cedex, Francia
- 1160.47.3301B Boehringer Ingelheim Investigational Site
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Brest Cedex, Francia
- 1160.47.3301C Boehringer Ingelheim Investigational Site
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Brest Cedex, Francia
- 1160.47.3301D Boehringer Ingelheim Investigational Site
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Brest Cedex, Francia
- 1160.47.3301E Boehringer Ingelheim Investigational Site
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Brest Cedex, Francia
- 1160.47.3301F Boehringer Ingelheim Investigational Site
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Brest Cedex, Francia
- 1160.47.3301H Boehringer Ingelheim Investigational Site
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Brest Cedex, Francia
- 1160.47.3301I Boehringer Ingelheim Investigational Site
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Lorient, Francia
- 1160.47.3302A Boehringer Ingelheim Investigational Site
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St Etienne Cedex 2, Francia
- 1160.47.3303A Boehringer Ingelheim Investigational Site
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St Etienne Cedex 2, Francia
- 1160.47.3303B Boehringer Ingelheim Investigational Site
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St Etienne Cedex 2, Francia
- 1160.47.3303C Boehringer Ingelheim Investigational Site
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St Etienne Cedex 2, Francia
- 1160.47.3303D Boehringer Ingelheim Investigational Site
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Vandoeuvre les Nancy, Francia
- 1160.47.3308A Boehringer Ingelheim Investigational Site
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Athens, Grecia
- 1160.47.30001 Boehringer Ingelheim Investigational Site
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Athens, Grecia
- 1160.47.30006 Boehringer Ingelheim Investigational Site
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Athens, Grecia
- 1160.47.30007 Boehringer Ingelheim Investigational Site
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Athens, Grecia
- 1160.47.30009 Boehringer Ingelheim Investigational Site
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Budapest, Hungría
- 1160.47.36001 Boehringer Ingelheim Investigational Site
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Budapest, Hungría
- 1160.47.36006 Boehringer Ingelheim Investigational Site
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Budapest, Hungría
- 1160.47.36007 Boehringer Ingelheim Investigational Site
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Debrecen, Hungría
- 1160.47.36002 Boehringer Ingelheim Investigational Site
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Gyula, Hungría
- 1160.47.36012 Boehringer Ingelheim Investigational Site
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Miskolc, Hungría
- 1160.47.36004 Boehringer Ingelheim Investigational Site
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Pecs, Hungría
- 1160.47.36003 Boehringer Ingelheim Investigational Site
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Szombathely, Hungría
- 1160.47.36011 Boehringer Ingelheim Investigational Site
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Székesfehérvár, Hungría
- 1160.47.36010 Boehringer Ingelheim Investigational Site
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Ahmedabad, India
- 1160.47.91002 Boehringer Ingelheim Investigational Site
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Bangalore, India
- 1160.47.91011 Boehringer Ingelheim Investigational Site
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Bangalore, India
- 1160.47.91015 Boehringer Ingelheim Investigational Site
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Chennai, India
- 1160.47.91012 Boehringer Ingelheim Investigational Site
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Chennai, India
- 1160.47.91017 Boehringer Ingelheim Investigational Site
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Madurai, India
- 1160.47.91009 Boehringer Ingelheim Investigational Site
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Mysore, India
- 1160.47.91007 Boehringer Ingelheim Investigational Site
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New Delhi, India
- 1160.47.91003 Boehringer Ingelheim Investigational Site
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New Delhi, India
- 1160.47.91010 Boehringer Ingelheim Investigational Site
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Pune, India
- 1160.47.91001 Boehringer Ingelheim Investigational Site
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Pune, India
- 1160.47.91005 Boehringer Ingelheim Investigational Site
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Pune, India
- 1160.47.91008 Boehringer Ingelheim Investigational Site
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Trivandrum, India
- 1160.47.91014 Boehringer Ingelheim Investigational Site
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Vadodara, India
- 1160.47.91004 Boehringer Ingelheim Investigational Site
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new Delhi, India
- 1160.47.91006 Boehringer Ingelheim Investigational Site
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Afula, Israel
- 1160.47.97202 Boehringer Ingelheim Investigational Site
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Ashkelon, Israel
- 1160.47.97207 Boehringer Ingelheim Investigational Site
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Haifa, Israel
- 1160.47.97211 Boehringer Ingelheim Investigational Site
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Holon, Israel
- 1160.47.97203 Boehringer Ingelheim Investigational Site
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Kfar Saba, Israel
- 1160.47.97205 Boehringer Ingelheim Investigational Site
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Petach Tikva, Israel
- 1160.47.97206 Boehringer Ingelheim Investigational Site
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Rehovot, Israel
- 1160.47.97208 Boehringer Ingelheim Investigational Site
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Tel Aviv, Israel
- 1160.47.97210 Boehringer Ingelheim Investigational Site
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Tel Hashomer, Israel
- 1160.47.97204 Boehringer Ingelheim Investigational Site
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Zerifin, Israel
- 1160.47.97201 Boehringer Ingelheim Investigational Site
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Bologna, Italia
- 1160.47.39003 Boehringer Ingelheim Investigational Site
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Cremona, Italia
- 1160.47.39004 Boehringer Ingelheim Investigational Site
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Genova, Italia
- 1160.47.39006 Boehringer Ingelheim Investigational Site
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Milano, Italia
- 1160.47.39008 Boehringer Ingelheim Investigational Site
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Reggio Emilia, Italia
- 1160.47.39007 Boehringer Ingelheim Investigational Site
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Udine, Italia
- 1160.47.39009 Boehringer Ingelheim Investigational Site
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Vittorio Veneto, Italia
- 1160.47.39005 Boehringer Ingelheim Investigational Site
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Chihuahua, México
- 1160.47.52036 Boehringer Ingelheim Investigational Site
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Culiacan, México
- 1160.47.52039 Boehringer Ingelheim Investigational Site
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Guadalajara, Jal., México
- 1160.47.52030 Boehringer Ingelheim Investigational Site
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Monterrey, México
- 1160.47.52027 Boehringer Ingelheim Investigational Site
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San Luis Potosí, México
- 1160.47.52034 Boehringer Ingelheim Investigational Site
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Oslo, Noruega
- 1160.47.47001 Boehringer Ingelheim Investigational Site
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Oslo, Noruega
- 1160.47.47004 Boehringer Ingelheim Investigational Site
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Rud, Noruega
- 1160.47.47003 Boehringer Ingelheim Investigational Site
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Trondheim, Noruega
- 1160.47.47005 Boehringer Ingelheim Investigational Site
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Christchurch, Nueva Zelanda
- 1160.47.64004 Boehringer Ingelheim Investigational Site
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Grafton, Nueva Zelanda
- 1160.47.64003 Boehringer Ingelheim Investigational Site
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Otahuhu, Nueva Zelanda
- 1160.47.64002 Boehringer Ingelheim Investigational Site
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Takapuna Auckland 9, Nueva Zelanda
- 1160.47.64001 Boehringer Ingelheim Investigational Site
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Ankara, Pavo
- 1160.47.90003 Boehringer Ingelheim Investigational Site
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Ankara, Pavo
- 1160.47.90004 Boehringer Ingelheim Investigational Site
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Ankara, Pavo
- 1160.47.90005 Boehringer Ingelheim Investigational Site
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Istanbul, Pavo
- 1160.47.90001 Boehringer Ingelheim Investigational Site
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Istanbul, Pavo
- 1160.47.90002 Boehringer Ingelheim Investigational Site
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Istanbul, Pavo
- 1160.47.90007 Boehringer Ingelheim Investigational Site
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Izmir, Pavo
- 1160.47.90006 Boehringer Ingelheim Investigational Site
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Amersfoort, Países Bajos
- 1160.47.31001 Boehringer Ingelheim Investigational Site
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Amsterdam, Países Bajos
- 1160.47.31006 Boehringer Ingelheim Investigational Site
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Amsterdam, Países Bajos
- 1160.47.31007 Boehringer Ingelheim Investigational Site
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Den Bosch, Países Bajos
- 1160.47.31010 Boehringer Ingelheim Investigational Site
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Heerlen, Países Bajos
- 1160.47.31014 Boehringer Ingelheim Investigational Site
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Maastricht, Países Bajos
- 1160.47.31005 Boehringer Ingelheim Investigational Site
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Rotterdam, Países Bajos
- 1160.47.31004 Boehringer Ingelheim Investigational Site
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Rotterdam, Países Bajos
- 1160.47.31009 Boehringer Ingelheim Investigational Site
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Kielce, Polonia
- 1160.47.48004 Boehringer Ingelheim Investigational Site
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Krakow, Polonia
- 1160.47.48005 Boehringer Ingelheim Investigational Site
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Krakow, Polonia
- 1160.47.48007 Boehringer Ingelheim Investigational Site
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Poznan, Polonia
- 1160.47.48003 Boehringer Ingelheim Investigational Site
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Warsaw, Polonia
- 1160.47.48006 Boehringer Ingelheim Investigational Site
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Beijing, Porcelana
- 1160.47.86001 Boehringer Ingelheim Investigational Site
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Beijing, Porcelana
- 1160.47.86015 Boehringer Ingelheim Investigational Site
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Chengdu, Porcelana
- 1160.47.86014 Boehringer Ingelheim Investigational Site
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Guangzhou, Porcelana
- 1160.47.86012 Boehringer Ingelheim Investigational Site
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Hangzhou, Porcelana
- 1160.47.86009 Boehringer Ingelheim Investigational Site
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Hangzhou, Porcelana
- 1160.47.86010 Boehringer Ingelheim Investigational Site
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Nanjing, Porcelana
- 1160.47.86013 Boehringer Ingelheim Investigational Site
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Shanghai, Porcelana
- 1160.47.86002 Boehringer Ingelheim Investigational Site
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Shanghai, Porcelana
- 1160.47.86003 Boehringer Ingelheim Investigational Site
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Shanghai, Porcelana
- 1160.47.86004 Boehringer Ingelheim Investigational Site
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Shanghai, Porcelana
- 1160.47.86005 Boehringer Ingelheim Investigational Site
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Shanghai, Porcelana
- 1160.47.86006 Boehringer Ingelheim Investigational Site
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Shanghai, Porcelana
- 1160.47.86007 Boehringer Ingelheim Investigational Site
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Shanghai, Porcelana
- 1160.47.86016 Boehringer Ingelheim Investigational Site
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Shijiazhuang, Porcelana
- 1160.47.86011 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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Headington, Oxford, Reino Unido
- 1160.47.44005 Boehringer Ingelheim Investigational Site
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London, Reino Unido
- 1160.47.44009 Boehringer Ingelheim Investigational Site
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London, Reino Unido
- 1160.47.44011 Boehringer Ingelheim Investigational Site
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Newcastle upon Tyne, Reino Unido
- 1160.47.44006 Boehringer Ingelheim Investigational Site
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Sheffield, Reino Unido
- 1160.47.44012 Boehringer Ingelheim Investigational Site
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Brno, República Checa
- 1160.47.42001 Boehringer Ingelheim Investigational Site
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Hradec Kralove, República Checa
- 1160.47.42002 Boehringer Ingelheim Investigational Site
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Hranice, República Checa
- 1160.47.42011 Boehringer Ingelheim Investigational Site
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Liberec, República Checa
- 1160.47.42012 Boehringer Ingelheim Investigational Site
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Novy Jicin, República Checa
- 1160.47.42015 Boehringer Ingelheim Investigational Site
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Ostrava-Vitkovice, República Checa
- 1160.47.42005 Boehringer Ingelheim Investigational Site
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Praha 2, República Checa
- 1160.47.42004 Boehringer Ingelheim Investigational Site
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Tabor, República Checa
- 1160.47.42014 Boehringer Ingelheim Investigational Site
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Usti nad Labem, República Checa
- 1160.47.42010 Boehringer Ingelheim Investigational Site
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Zlin, República Checa
- 1160.47.42007 Boehringer Ingelheim Investigational Site
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Johannesburg, Sudáfrica
- 1160.47.27001 Boehringer Ingelheim Investigational Site
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Johannesburg, Sudáfrica
- 1160.47.27002 Boehringer Ingelheim Investigational Site
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Johannesburg, Sudáfrica
- 1160.47.27006 Boehringer Ingelheim Investigational Site
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Pretoria, Sudáfrica
- 1160.47.27007
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Randburg, Sudáfrica
- 1160.47.27003 Boehringer Ingelheim Investigational Site
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Roodepoort, Sudáfrica
- 1160.47.27005 Boehringer Ingelheim Investigational Site
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Göteborg, Suecia
- 1160.47.46002 Boehringer Ingelheim Investigational Site
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Jönköping, Suecia
- 1160.47.46006 Boehringer Ingelheim Investigational Site
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Stockholm, Suecia
- 1160.47.46001 Boehringer Ingelheim Investigational Site
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Stockholm, Suecia
- 1160.47.46007 Boehringer Ingelheim Investigational Site
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Stockholm, Suecia
- 1160.47.46008 Boehringer Ingelheim Investigational Site
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Sundsvall, Suecia
- 1160.47.46005 Boehringer Ingelheim Investigational Site
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Uppsala, Suecia
- 1160.47.46003 Boehringer Ingelheim Investigational Site
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Kharkov, Ucrania
- 1160.47.38002 Boehringer Ingelheim Investigational Site
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Kiev, Ucrania
- 1160.47.38006 Boehringer Ingelheim Investigational Site
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Vinnitsa, Ucrania
- 1160.47.38005 Boehringer Ingelheim Investigational Site
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Zaporozhye, Ucrania
- 1160.47.38003 Boehringer Ingelheim Investigational Site
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Criterios de participación
Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.
Criterio de elegibilidad
Edades elegibles para estudiar
18 años y mayores (Adulto, Adulto Mayor)
Acepta Voluntarios Saludables
No
Géneros elegibles para el estudio
Todos
Descripción
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)
Plan de estudios
Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Doble
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
|
Experimental: Dabigatran
Patient to receive 1 capsule containing dabigatran 150 mg twice daily plus placebo tablets for warfarin as decided by sham INR measurements
|
Dabigatran 150 mg BID (twice daily)
|
|
Comparador activo: 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
|
Warfarin dosed individually to maintain INR 2.0-3.0
|
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Composite of Recurrent VTE or VTE Death at 36 Months
Periodo de tiempo: 36 months
|
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.
|
36 months
|
|
Composite of Recurrent VTE or VTE Death at 18 Months
Periodo de tiempo: 18 months
|
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.
|
18 months
|
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Composite of Recurrent VTE or All Cause Death at 36 Months
Periodo de tiempo: 36 months
|
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.
|
36 months
|
|
Composite of Recurrent VTE or All Cause Death at 18 Months
Periodo de tiempo: 18 months
|
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
Periodo de tiempo: 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
|
|
DVT at 18 Months
Periodo de tiempo: 18 months
|
Symptomatic Deep vein thrombosis (DVT).
All DVT events required objective verification through definitive diagnostic evaluation.
|
18 months
|
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Symptomatic Pulmonary Embolism (PE) at 36 Months
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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.
|
36 months
|
|
Deaths Related to VTE at 18 Months
Periodo de tiempo: 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.
|
18 months
|
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Deaths of All Causes at 36 Months
Periodo de tiempo: 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.
|
36 months
|
|
Deaths of All Causes at 18 Months
Periodo de tiempo: 18 months
|
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.
|
18 months
|
|
Number of Participants With Bleeding Events
Periodo de tiempo: 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
|
first intake of study drug until 6 days following last intake of study drug
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Laboratory Analysis
Periodo de tiempo: 18 months + 30 days follow up
|
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
|
|
Number of Participants With Definite Acute Coronary Syndrome (ACS)
Periodo de tiempo: 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
|
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.
|
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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Colaboradores e Investigadores
Aquí es donde encontrará personas y organizaciones involucradas en este estudio.
Patrocinador
Publicaciones y enlaces útiles
La persona responsable de ingresar información sobre el estudio proporciona voluntariamente estas publicaciones. Estos pueden ser sobre cualquier cosa relacionada con el estudio.
Publicaciones Generales
- 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.
Enlaces Útiles
Fechas de registro del estudio
Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.
Fechas importantes del estudio
Inicio del estudio
1 de mayo de 2006
Finalización primaria (Actual)
1 de octubre de 2010
Fechas de registro del estudio
Enviado por primera vez
23 de mayo de 2006
Primero enviado que cumplió con los criterios de control de calidad
23 de mayo de 2006
Publicado por primera vez (Estimar)
24 de mayo de 2006
Actualizaciones de registros de estudio
Última actualización publicada (Estimar)
19 de mayo de 2014
Última actualización enviada que cumplió con los criterios de control de calidad
8 de mayo de 2014
Última verificación
1 de diciembre de 2013
Más información
Términos relacionados con este estudio
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- 1160.47
- 2005-002536-94 (Número EudraCT: EudraCT)
Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .