Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2026-03-26 @ 3:15 PM
Ignite Modification Date:
2026-03-26 @ 3:15 PM
NCT ID:
NCT07364266
Eligibility Criteria:
Inclusion Criteria:
* Adult patients at the time of amputation; Post-traumatic algodystrophy diagnosed clinically and confirmed by imaging if necessary, according to the Budapest criteria; Amputation performed for analgesic purposes, after failure of conventional medical and rehabilitation treatments; Postoperative follow-up carried out at CHRU de Brest, with available data on prosthetic fitting and postoperative activities; Complete medical record accessible via the hospital electronic medical record.
Exclusion Criteria:
* Patients amputated for another cause (vascular, tumor, infectious, etc.); Patients not followed after amputation or immediately lost to follow-up after surgery; Incomplete medical records regarding the main variables of interest (dates of amputation, prosthetic fitting, functional follow-up).
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT07364266
Study Brief:
Protocol Section:
NCT07364266