The Product Surveillance Registry REVERSE Post Approval Study
NCT01660035 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 155
Last updated 2022-04-18
Summary
The purpose of the REVERSE Post Approval Study (PAS) is to confirm the benefit observed in the REVERSE and RAFT pivotal studies in "real-world" clinical practice.
Conditions
Sponsors & Collaborators
- lead INDUSTRY
Eligibility
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2012-04-30
- Primary Completion
- 2022-04-30
- Completion
- 2022-04-30
Countries
- United States
- Belgium
- Canada
- France
- Germany
- Italy
- Netherlands
- Sweden
- Switzerland
- United Kingdom
Study Locations
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