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

NCT02934802 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 140

Last updated 2019-04-17

No results posted yet for this 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.

Conditions

  • Knee Arthroplasty

Interventions

DEVICE

Total Knee prothesis e motion PS Pro

Sponsors & Collaborators

  • BBraun Medical SAS

    lead INDUSTRY

Principal Investigators

  • François Boillot · Groupe hospitalier Paris-St Joseph

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-05-26
Primary Completion
2025-02-28
Completion
2025-02-28

Countries

  • France

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02934802 on ClinicalTrials.gov