Post-PMA Approval Study: 10 Year Follow-Up IDE Subjects
NCT00721994 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 231
Last updated 2018-11-21
Summary
primary endpoint of this Study is maintenance of "at least good clinical status" for a period of 10 years following initial implantation among Cormet procedures enrolled inthe pre-market IDE.
Conditions
- Osteoarthritis
- Avascular Necrosis
- Rheumatoid Arthritis
Interventions
- DEVICE
-
Cormet Hip Resurfacing System
Cormet Hip Resurfacing System
Sponsors & Collaborators
-
Corin
lead INDUSTRY
Principal Investigators
-
Kathy Trier, Ph.D. · Corin
Eligibility
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2008-05-31
- Primary Completion
- 2017-06-30
- Completion
- 2017-08-31
Countries
- United States
Study Locations
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