Reduced-dosed Rivaroxaban in the Long-term Prevention of Recurrent Symptomatic VTE(Venous Thromboembolism) (EinsteinChoice)
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.
Study Type: Interventional
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose: Prevention
Official Title: 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
Enrollment: 3396
Study Start Date: March 2014
Study Completion Date: November 2016
Primary Completion Date: September 2016 (Final data collection date for primary outcome measure)
Arms:
- Experimental: Arm 1
- Experimental: Arm 2
- Active Comparator: Arm 3
Related journal:
- Rivaroxaban or Aspirin for Extended Treatment of Venous Thromboembolism.
Category | Value |
---|---|
Date last updated at source | 2017-01-18 |
Study type(s) | Interventional |
Expected enrolment | 3396 |
Study start date | 2014-03-01 |
Estimated primary completion date | 2016-09-01 |