ROCC Knee Data Collection
Terminated
- Conditions
- Arthritis of Knee
- Interventions
- Device: Knee Replacement (with ROCC Knee prosthesis)
- Registration Number
- NCT00758901
- Lead Sponsor
- Zimmer Biomet
- 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
Recruitment & Eligibility
- Status
- TERMINATED
- Sex
- All
- Target Recruitment
- 200
Inclusion Criteria
Not provided
Exclusion Criteria
Not provided
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description 1 ROCC Knee prosthesis Knee Replacement (with ROCC Knee prosthesis) Consecutive series of patients with ROCC Knee prosthesis.
- Primary Outcome Measures
Name Time Method American Knee Score 3 months, 1yr, 2yr, 3yr, 4yr and 5 yr
- Secondary Outcome Measures
Name Time Method Complication Any time Patient Satisfaction 3 months, 1yr, 2yr, 3yr, 4yr and 5 yr
Trial Locations
- Locations (3)
Hospital Torrecardenas
🇪🇸Almeria, Spain
Clinique des Fontaines
🇫🇷Meulin, France
A. ö Landeskrankenhaus Gmunden
🇦🇹Gmunden, Austria