An extended study in the clinical evaluation of direct oral anticoagulants
Not Applicable
- Conditions
- Atrial fibrillation
- Registration Number
- JPRN-UMIN000050585
- Lead Sponsor
- Japan Science and Technology Agency
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up continuing
- Sex
- All
- Target Recruitment
- 6900
Inclusion Criteria
Not provided
Exclusion Criteria
Patients who are considered inappropriate to include in the study by physicians.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method all-cause death, myocardial infarction, stroke, bleeding, gastrointestinal symptoms, heart failure hospitalization, C-reactive protein, catheter ablation
- Secondary Outcome Measures
Name Time Method