Trials / Terminated
TerminatedNCT00758901
ROCC Knee Data Collection
A Prospective, Multicentre Study Evaluating the Clinical Performance of the ROCC Knee Prosthesis
- Status
- Terminated
- Phase
- —
- Study type
- Observational
- Enrollment
- 200 (actual)
- Sponsor
- Zimmer Biomet · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
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
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Knee Replacement (with ROCC Knee prosthesis) | Knee Replacement (with ROCC Knee prosthesis) |
Timeline
- Start date
- 2003-11-01
- Primary completion
- 2010-12-01
- Completion
- 2010-12-01
- First posted
- 2008-09-25
- Last updated
- 2017-03-10
Locations
3 sites across 3 countries: Austria, France, Spain
Source: ClinicalTrials.gov record NCT00758901. Inclusion in this directory is not an endorsement.