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 |
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
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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