CONSERVE Plus Post-Approval Study (PAS)
NCT01367899 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 199
Last updated 2014-10-28
Summary
The objective of this post-approval study is to provide scientifically valid and reliable evidence that supports claims of longer term safety and effectiveness with regard to Month 120 device survivorship rates.
Conditions
- Other and Unspecified Injury to Hip and Thigh
Sponsors & Collaborators
-
MicroPort Orthopedics Inc.
lead INDUSTRY
Principal Investigators
-
Michael Bolognesi, MD · Duke University
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2010-11-30
- Primary Completion
- 2014-09-30
- Completion
- 2014-09-30
Countries
- United States
Study Locations
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