Outcome of a Cohort of Patients Fitted With a SYME Type Prosthesis in the Context of a Hindfoot Amputation With Distal Support

NCT06448260 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 94

Last updated 2025-04-16

No results posted yet for this study

Summary

The purpose of this study is to see outcome of patients with syme prothesis in order to comment the handfoot amputation.

Conditions

  • Amputation, Surgical
  • Walking, Difficulty

Interventions

OTHER

Questionnary

Data from theses patients will be collected in our personnal data base with ask of consent according to the law Then each patient alive will have questionnary to answer by phone or during a visit.

Sponsors & Collaborators

  • Institut Robert Merle d'aubigné

    lead OTHER

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-05-20
Primary Completion
2024-07-31
Completion
2024-09-30

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 NCT06448260 on ClinicalTrials.gov