Dabigatran Etexilate for Stroke Prevention in Patients With Atrial Fibrillation and Mild to Moderate Renal Impairment
- Conditions
- Atrial Fibrillation
- Registration Number
- NCT01721837
- Lead Sponsor
- Boehringer Ingelheim
- Brief Summary
Non-interventional, observational study of physicians' use of Dabigatran etexilate for stroke prevention in patients with atrial fibrillation and mild to moderate renal impairment
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 4340
Not provided
Not provided
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Creatinine Clearance (Recalculated Using Entries of Age, Gender, Body Weight and Serum Creatinine Made by the Physician) One single observation time point: at the time of prescription before the first intake of dabigatran etexilate The creatinine clearance was recalculated with the Cockcroft-Gault formula using age, gender, body weight, and serum creatinine.
- Secondary Outcome Measures
Name Time Method
Related Research Topics
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Trial Locations
- Locations (1616)
Boehringer Ingelheim Investigational Site 626
🇩🇪Aachen, Germany
Boehringer Ingelheim Investigational Site 627
🇩🇪Aachen, Germany
Boehringer Ingelheim Investigational Site 642
🇩🇪Aachen, Germany
Boehringer Ingelheim Investigational Site 643
🇩🇪Aachen, Germany
Boehringer Ingelheim Investigational Site 156
🇩🇪Aalen, Germany
Boehringer Ingelheim Investigational Site 159
🇩🇪Aalen, Germany
Boehringer Ingelheim Investigational Site 472
🇩🇪Aarbergen, Germany
Boehringer Ingelheim Investigational Site 842
🇩🇪Ahaus-Alstaette, Germany
Boehringer Ingelheim Investigational Site 830
🇩🇪Ahaus, Germany
Boehringer Ingelheim Investigational Site 834
🇩🇪Ahaus, Germany
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