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

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

94 participants

Study Classification

OBSERVATIONAL

Study Start Date

2024-05-20

Study Completion Date

2024-09-30

Brief Summary

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

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Detailed Description

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Conditions

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Amputation, Surgical Walking, Difficulty

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

PROSPECTIVE

Study Groups

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Patient with ATCT

Patient with tibiocalcaneal arthrodesis with talectomy amputation

Questionnary

Intervention Type OTHER

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.

Interventions

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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.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Syme or Pirogoff or ATCT or arthrodesized Chopart type amputation
* Age \> 18 years old,
* First fitting or renewal of Syme type prosthesis delivered to IRMA between January 2008 and December 2018