PS150 Total Knee Arthroplasty Outcomes Registry

DePuy Synthes

Status: Completed

Conditions: Osteoarthritis; Rheumatoid Arthritis

Treatments: Device: P.F.C. Sigma PS150 RP Total Knee System

Study type: Observational

Funder types: Industry

Identifiers

NCT02319291

13004

Details and patient eligibility

About

This registry is intended to evaluate the clinical outcomes of the DePuy P.F.C. Sigma PS150 RP Total Knee System. 200 participants will be enrolled prospectively or retrospectively and the follow up period will be 5 years. Data collection will include Radiographic Analysis, Knee Society Evaluation and Adverse Events.

Enrollment: 175 patients

Sex: All

Volunteers: No Healthy Volunteers

Inclusion criteria

• Primary total knee replacement for any indication in accordance with the Instructions For Use accompanying the SIGMA PS150 implant.
• Signed Informed Patient Consent

Exclusion criteria

• There are no exclusion criteria for this registry.

Trial design

175 participants in 1 patient group

Participants

Description:

P.F.C. Sigma PS150 RP Total Knee System

Treatment:

Device: P.F.C. Sigma PS150 RP Total Knee System