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

I

Institut Robert Merle d'aubigné

Status

Completed

Conditions

Amputation, Surgical
Walking, Difficulty

Treatments

Other: Questionnary

Study type

Observational

Funder types

Other

Identifiers

NCT06448260
2024-A00393-44

Details and patient eligibility

About

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

Enrollment

94 patients

Sex

All

Volunteers

No 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.

Trial design

94 participants in 1 patient group

Patient with ATCT
Description:
Patient with tibiocalcaneal arthrodesis with talectomy amputation
Treatment:
Other: Questionnary

Trial contacts and locations

1

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Central trial contact

Anton M KANIEWSKI, MD

Data sourced from clinicaltrials.gov

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