Outcome of a Cohort of Patients Fitted With a SYME Type Prosthesis in the Context of a Hindfoot Amputation With Distal Support
Sponsored by Institut Robert Merle d'aubigné
About this trial
Last updated 8 months ago
Study ID
2024-A00393-44
Status
Recruiting
Type
Observational [Patient Registry]
Placebo
No
Accepting
All
All
Not accepting
Healthy Volunteers
Trial Timing
Ended 9 months ago
What is this trial about?
The purpose of this study is to see outcome of patients with syme prothesis in order to
comment the handfoot amputation.
What are the participation requirements?
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.
Locations
Location
Status
Recruiting