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The purpose of this study is to demonstrate that the efficacy and safety of 20 mg once daily rivaroxaban in preventing thromboembolic events in subjects with atrial fibrillation not related to mitral valve stenosis. E-mail: [email protected]. Share Facebook Twitter LinkedIn. Bayer Identifier: View results Ask a Question. Key Participation Requirements sex. Inclusion Criteria - Male and female pa. Inclusion Criteria - Male and female patients 18 years of age or older - Subjects must have documented atrial fibrillation on 2 separate occasions within 6 months before screening - History of a prior stroke, transient ischemic attack or non-neurologic systemic embolism believed to be cardiac in origin, OR at least two of the following risk factors: -- Heart failure -- Hypertension -- Age 75 years or greater -- Diabetes mellitus Exclusion Criteria - Significant mitral stenosis - Transient atrial fibrillation caused by a reversible disorder - Active internal bleeding - Severe disabling stroke - History of intracranial bleeding - Hemorrhagic disorders.
Trial Summary Enrollment Goal Trial Dates December September Phase 3. Could I receive a placebo? Accepts Healthy Volunteers No. Where to Participate Loading Ask a Question. Locations Locations. Intervention Type : Drug. Trial Purpose : Prevention. Allocation : Randomized. Blinding : Double Blind. Assignment : Parallel Assignment. Trial Arms : 2. Click here and search for drug information provided by the FDA.
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