Pradaxa (Dabigatran Etexilate) 150 mg/q.d. in Patients With Moderate Renal Impairment After Hip or Knee Replacement Surgery
NCT00847301 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 472
Last updated 2015-09-25
Summary
An observational cohort study on safety and efficacy to generate additional data on the benefit/risk profile of the 150 mg dose of Pradaxa in patients with renal impairment
Conditions
- Arthroplasty, Replacement
- Thromboembolism
Sponsors & Collaborators
- lead INDUSTRY
Principal Investigators
-
Boehringer Ingelheim · Boehringer Ingelheim
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2009-04-30
- Primary Completion
- 2014-07-31
- Completion
- 2014-07-31
Countries
- Austria
- France
- Germany
- Italy
- Spain
- Sweden
- United Kingdom
Study Locations
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