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Dabigatran Etexilate for Stroke Prevention in Patients With Atrial Fibrillation and Mild to Moderate Renal Impairment

Completed
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
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
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
NameTimeMethod

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

Scroll for more (1606 remaining)
Boehringer Ingelheim Investigational Site 626
🇩🇪Aachen, Germany

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