Non-Interventional Consecutive and Prospective Study of e.Motion® PS Pro Prosthesis in the Total Knee Artroplasty

B. Braun

Status: Enrolling

Conditions: Knee Arthroplasty

Treatments: Device: Total Knee prothesis e motion PS Pro

Study type: Observational

Funder types: Industry

Identifiers

NCT02934802

AAG-O-H-1420

Details and patient eligibility

About

This post-market clinical follow-up study intends to investigate the survival rate at 5 years of the e.motion® PS Pro System.

Enrollment: 140 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Patient having signed informed consent
• Patients over 18 for which a Total Knee Prosthesis with e.motion® PS Pro was decided
• Patients willing to participate in a 5 years follow-up

Exclusion criteria

• Active or suspected infection
• Tumor on the concerned knee
• Patient vulnerable and under legal protection