Total Knee Replacement With the ROCC Knee

Bercovy, Michel, M.D.

Status: Completed

Conditions: Osteoarthritis; Rheumatoid Arthritis

Treatments: Device: Total knee replacement with the ROCC® knee prosthesis

Study type: Interventional

Identifiers

NCT02127619

602-ROCC

Details and patient eligibility

About

The purpose of this study was to assess the results of a Total Knee prosthesis specifically intended to enhance functional performance , especially in terms of physical and sports activity.

Full description

Clinical and radiographic results , complications, early post-operative and late functional outcome and survivorship were studied in a continuous prospective series of 500 patients ( 602 knees) managed using the ROCC knee ( BIOMET INC - Warsaw- IND, USA).

A minimum follow-up of 5 years was required.

Enrollment: 500 patients

Sex: All

Ages: 42 to 90 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• all patients receiving a total knee

Exclusion criteria

• patients with severe psychiatric, neurologic, cardiologic or locomotor pathology occuring after the total knee replacement

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)