ROCC Knee Data Collection
NCT00758901 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 200
Last updated 2017-03-10
Summary
This observational study intends to collect efficacy and safety data on ROCC Knee system.
Conditions
- Arthritis of Knee
Interventions
- DEVICE
-
Knee Replacement (with ROCC Knee prosthesis)
Knee Replacement (with ROCC Knee prosthesis)
Sponsors & Collaborators
-
Biomet France SARL
collaborator INDUSTRY -
Zimmer Biomet
lead INDUSTRY
Principal Investigators
-
Michel BERCOVY, MD · Clinique des Fontaines
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2003-11-30
- Primary Completion
- 2010-12-31
- Completion
- 2010-12-31
Countries
- Austria
- France
- Spain
Study Locations
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