Xarelto for VTE Prophylaxis After Hip or Knee Arthroplasty
NCT00831714 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 19076
Last updated 2017-01-23
Summary
The main goal is to provide additional information to the risk-benefit assessment of the drug.
Conditions
- Venous Thromboembolism
Interventions
- DRUG
-
Rivaroxaban (Xarelto, BAY59-7939)
Female and male patients, who are at least 18 years of age and will undergo elective hip or knee arthroplasty, after the decision for VTE prophylaxis with Rivaroxaban has been made
- DRUG
-
Standard care treatment for VTE prophylaxis
Female and male patients, who are at least 18 years of age and will undergo elective hip or knee arthroplasty, after the decision for a pharmacologic VTE prophylaxis treatment other than rivaroxaban has been made
Sponsors & Collaborators
-
Janssen Research & Development, LLC
collaborator INDUSTRY - lead INDUSTRY
Principal Investigators
-
Bayer Study Director · Bayer
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2009-02-28
- Primary Completion
- 2011-06-30
- Completion
- 2013-04-30
Countries
- Australia
- Austria
- Belgium
- Bosnia and Herzegovina
- Brazil
- Canada
- Chile
- China
- Colombia
- Cyprus
- Czechia
- Denmark
- Estonia
- Finland
- France
- Germany
- Greece
- Hong Kong
- Hungary
- India
- Italy
- Latvia
- Lebanon
- Lithuania
- Mexico
- Netherlands
- North Macedonia
- Norway
- Philippines
- Portugal
- Serbia
- Singapore
- Slovakia
- South Africa
- South Korea
- Spain
- Sweden
- Switzerland
- United Arab Emirates
- United Kingdom
- Venezuela
- Vietnam
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