Reduced-dosed Rivaroxaban in the Long-term Prevention of Recurrent Symptomatic VTE(Venous Thromboembolism)



Status:Completed
Conditions:Cardiology, Cardiology, Cardiology, Cardiology, Cardiology, Cardiology
Therapuetic Areas:Cardiology / Vascular Diseases
Healthy:No
Age Range:18 - Any
Updated:12/21/2017
Start Date:March 5, 2014
End Date:November 4, 2016

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Reduced-dosed Rivaroxaban and Standard-dosed Rivaroxaban Versus ASA in the Long-term Prevention of Recurrent Symptomatic Venous Thromboembolism in Patients With Symptomatic Deep-vein Thrombosis and/or Pulmonary Embolism

This is a multicenter, randomized, double-blind, event-driven, superiority study for
efficacy.

Patients with confirmed symptomatic DVT (Deep Vein Thrombosis) or PE (Pulmonary embolism) who
completed 6 or 12 months of treatment of anticoagulation are eligible for this trial


Inclusion Criteria:

- Patients with confirmed symptomatic PE and/or DVT who have been treated for 6 to 12
months and did not interrupt anticoagulation for longer than 1 week

Exclusion Criteria:

- Legal lower age limitations (country specific) Indication for therapeutic-dosed
anticoagulants Indication for antiplatelet therapy or a conventional non-steroid
anti-inflammatory drug (NSAID) Hepatic disease which is associated with coagulopathy
leading to a clinically relevant bleeding risk Calculated creatinine clearance < 30
mL/min
We found this trial at
24
sites
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Bellevue, WA
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Beverly Hills, California 90211
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Beverly Hills, CA
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Jacksonville, FL
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Joliet, IL
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Philadelphia, PA
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Rockport, ME
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San Antonio, TX
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Seattle, WA
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Spokane, WA
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Tacoma, WA
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Toledo, OH
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Ventura, CA
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