Observational Study to Evaluate Safety and Performance of the Total Ankle Prosthesis, EasyMove®

NCT04944576 · Status: ACTIVE_NOT_RECRUITING · Type: OBSERVATIONAL · Enrollment: 82

Last updated 2024-05-31

No results posted yet for this study

Summary

This study is a post-market clinical follow-up conducted in order to collect long-term data on safety and performance of the EasyMove prosthesis, which is intended to be implanted in case of total ankle replacement, when used in real life conditions according to the instructions for use.

Conditions

  • Ankle Injuries and Disorders

Interventions

DEVICE

Total Ankle Prosthesis, EasyMove®

Patients who will be implanted with a total ankle prosthesis, EasyMove.

Sponsors & Collaborators

  • FH ORTHO

    lead INDUSTRY

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-09-14
Primary Completion
2029-09-13
Completion
2029-09-13

Countries

  • France
  • Switzerland

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 NCT04944576 on ClinicalTrials.gov