NCT00758901
Terminated
Not Applicable
A Prospective, Multicentre Study Evaluating the Clinical Performance of the ROCC Knee Prosthesis
ConditionsArthritis of Knee
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Arthritis of Knee
- Sponsor
- Zimmer Biomet
- Enrollment
- 200
- Locations
- 3
- Primary Endpoint
- American Knee Score
- Status
- Terminated
- Last Updated
- 9 years ago
Overview
Brief Summary
This observational study intends to collect efficacy and safety data on ROCC Knee system.
Detailed Description
The ROCC® prosthesis is a rotating platform with: * Highly congruent surface contact, * NON CONSTRAINED kinematics allowing posterior roll back until 110° then anterior in hyperflexion like a normal knee * Allowing asymmetric movement
Investigators
Eligibility Criteria
Inclusion Criteria
- Not provided
Exclusion Criteria
- Not provided
Outcomes
Primary Outcomes
American Knee Score
Time Frame: 3 months, 1yr, 2yr, 3yr, 4yr and 5 yr
Secondary Outcomes
- Complication(Any time)
- Patient Satisfaction(3 months, 1yr, 2yr, 3yr, 4yr and 5 yr)
Study Sites (3)
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