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

Last updated: April 16, 2019
Sponsor: BBraun Medical SAS
Overall Status: Active - Recruiting

Phase

N/A

Condition

Knee Surgery

Knee Replacement

Treatment

N/A

Clinical Study ID

NCT02934802
AAG-O-H-1420
  • Ages > 18
  • All Genders

Study Summary

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

Eligibility Criteria

Inclusion

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

Exclusion Criteria:

  • Active or suspected infection

  • Tumor on the concerned knee

  • Patient vulnerable and under legal protection

Study Design

Total Participants: 140
Study Start date:
May 26, 2016
Estimated Completion Date:
February 28, 2025

Connect with a study center

  • Groupe hospitalier Paris-St Joseph

    Paris, 75014
    France

    Active - Recruiting

Not the study for you?

Let us help you find the best match. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.