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

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT06448260

Acronym

DEVSYME

Enrollment

Registered

2024-06-07

Start date

2024-05-20

Completion date

2024-09-30

Last updated

2025-04-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Amputation, Surgical, Walking, Difficulty

Keywords

Amputation, Prothesis, Outcome

Brief summary

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

Interventions

OTHERQuestionnary

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.

Study design

Observational model

CASE_CONTROL

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Healthy volunteers

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.

Design outcomes

Primary

Measure	Time frame	Description
The possibility of walking without a prosthesis	Immediatly after inclusion	Yes / No
Walking perimeter with prosthesis	Immediatly after inclusion	In meters
Number of re-amputation since first amputation	Immediatly after inclusion	—

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026