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:
2025-12-24 @ 10:44 PM
Ignite Modification Date:
2025-12-24 @ 10:44 PM
NCT ID:
NCT05034835
Eligibility Criteria:
Inclusion Criteria:
* Patients with CRPS of the upper limb with neuropathic pain
* Diagnosis of CRPS according to the Budapest criteria
* Diagnosis of neuropathic pain according to DN4
* CRPS evolving for more than 3 months
* No phlebitis or open sores on the upper limbs
* Patient consent to participate in the study
* No modification of his drug treatment for 1 month
* Affiliation to a social security scheme or beneficiary of such a scheme
Exclusion Criteria:
* Patient under guardianship, curatorship or safeguard of justice
* Psychiatric pathology altering the ability to consent
* Severe cognitive disorders that do not allow the patient to assess his pain
* Skin pathology preventing the wearing of the compression garment
* Patient who has previously worn a compression garment
* History of vascular disorders of the upper limbs, lymph node dissection, or any other pathology that can lead to edema regardless of CRPS
* Known allergy to one of the components of the compression garments of the Cerecare brand
* Declared pregnancy, breastfeeding woman or woman of childbearing potential without contraception
* Inability to put on the compression garment alone
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT05034835
Study Brief:
Protocol Section:
NCT05034835