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ROCC Knee Data Collection

Terminated
Conditions
Arthritis of Knee
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
Primary Outcome Measures
NameTimeMethod
American Knee Score3 months, 1yr, 2yr, 3yr, 4yr and 5 yr
Secondary Outcome Measures
NameTimeMethod
ComplicationAny time
Patient Satisfaction3 months, 1yr, 2yr, 3yr, 4yr and 5 yr

Trial Locations

Locations (3)

A. ö Landeskrankenhaus Gmunden

🇦🇹

Gmunden, Austria

Clinique des Fontaines

🇫🇷

Meulin, France

Hospital Torrecardenas

🇪🇸

Almeria, Spain

A. ö Landeskrankenhaus Gmunden
🇦🇹Gmunden, Austria
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