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:
NCT07361692
Eligibility Criteria:
Inclusion Criteria:
* Major
* Clinically active or active complex regional pain syndrome (CRPS) with positive Budapest criteria
* Scintigraphy showing signs consistent with CRPS
* Being affiliated with or a beneficiary of a social security scheme
Exclusion Criteria:
* Algodystrophy no longer meeting the Budapest criteria
* Relative contraindication to tDCS: psychosis (including treated psychosis), uncontrolled epilepsy, large scalp scar, intracerebral/intracranial metallic body
* Pregnant or breastfeeding women
* Minors
* Persons under legal protection (guardianship, conservatorship, and protective supervision)
* Persons deprived of their liberty by judicial or administrative order
* Unwilling individuals who cannot give their consent or cannot return for scheduled visits according to the protocol
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT07361692
Study Brief:
Protocol Section:
NCT07361692