Status:
TERMINATED
ROCC Knee Data Collection
Lead Sponsor:
Zimmer Biomet
Collaborating Sponsors:
Biomet France SARL
Conditions:
Arthritis of Knee
Eligibility:
All Genders
18+ years
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 ...
Eligibility Criteria
Inclusion
- Patients suitable for Knee Replacement for:
- osteoarthritis,
- rheumatoid arthritis
- bone necrosis affecting two knee compartments,
- correction of genu varus, genu valgus or post-traumatic deformities,
- sequelae of prior procedures.
Exclusion
Key Trial Info
Start Date :
November 1 2003
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
December 1 2010
Estimated Enrollment :
200 Patients enrolled
Trial Details
Trial ID
NCT00758901
Start Date
November 1 2003
End Date
December 1 2010
Last Update
March 10 2017
Active Locations (3)
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1
A. ö Landeskrankenhaus Gmunden
Gmunden, Austria
2
Clinique des Fontaines
Meulin, France
3
Hospital Torrecardenas
Almería, Spain