VEGA System® Study in the Total Knee Arthroplasty

NCT02944409 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 125

Last updated 2019-04-17

No results posted yet for this study

Summary

This post-market clinical follow-up study intends to investigate long-term functionality of the VEGA System®. The design of the VEGA System® is meant to provide the patient with more knee mobility compared to their pre-operative state.The endpoint is the revision of at least one of the prosthesis components

Conditions

  • Knee Arthroplasty

Interventions

DEVICE

total knee prothesis VEGA System

total knee replacement

Sponsors & Collaborators

  • BBraun Medical SAS

    lead INDUSTRY

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-07-01
Primary Completion
2025-02-28
Completion
2025-02-28

Countries

  • France

Study Locations

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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 NCT02944409 on ClinicalTrials.gov