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

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

Completed

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Key information

Conditions

Amputation, Surgical Mobility Limitation Pathological Conditions, Signs and Symptoms Signs and Symptoms Walking, Difficulty

Sex eligibility

All sexes

Study type

Observational

Primary location

Institut Robert Merle d'Aubigné

Valenton, France

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Exclusion criteria

Refusal documented in the file that the data be used for scientific purposes,
Congenital etiology of the condition.

Treatment and study plan

Questionnary

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.

Primary outcomes

The possibility of walking without a prosthesis

Time frame: Immediatly after inclusion

Yes / No
Walking perimeter with prosthesis

Time frame: Immediatly after inclusion

In meters
Number of re-amputation since first amputation

Time frame: Immediatly after inclusion

Sponsors and collaborators

Lead sponsor

Institut Robert Merle d'aubigné

Other

Registry information

Acronym: DEVSYME

Important dates

Study start: 2024
Primary completion: 2024
Study completion: 2024
First posted: Jun 7, 2024
Registry last updated: Apr 16, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.

Completed