ROCC Knee Data Collection

Zimmer Biomet

Status: Terminated

Conditions: Arthritis of Knee

Treatments: Device: Knee Replacement (with ROCC Knee prosthesis)

Study type: Observational

Funder types: Industry

Identifiers

NCT00758901

BMET FR 03

Details and patient eligibility

About

This observational study intends to collect efficacy and safety data on ROCC Knee system.

Full 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

Enrollment: 200 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

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.

Trial design

200 participants in 1 patient group

1 ROCC Knee prosthesis

Description:

Consecutive series of patients with ROCC Knee prosthesis.

Treatment:

Device: Knee Replacement (with ROCC Knee prosthesis)