Informations générales (source: ClinicalTrials.gov)
Impact of Compression Garments on Neuropathic-looking Pain in Patients With Complex Regional Pain Syndrome (CRPS) of the Upper Limbs. (VECODON)
Interventional
N/A
Centre Mutualiste de Rééducation et de Réadaptation Fonctionnelles de Kerpape (Voir sur ClinicalTrials)
octobre 2021
janvier 2025
04 janvier 2025
The aim is to study another alternative for the treatment of pain in people with CRPS.
Indeed, the TRAB / Medullary occupational therapy department of the CMRRF in Kerpape used
compression garments to reduce edema when it was present.In the case of CRPS of the upper
limbs, gloves or compression sleeves are used to decrease the edema which is sometimes
associated, although they are not supported for this indication. In this context, our
clinical experience leads us to believe that there would also be some efficacy in
neuropathic pain, this improvement being regularly described by patients.This study is
expected to show a notable reduction in neuropathic pain thanks to the wearing of a
compression garment.
Etablissements
| Les établissements sans correspondance certaine dans le répertoire FINESS dont les données sont issues de ClinicalTrials.gov Origine et niveau de fiabilité des données | |||||
|---|---|---|---|---|---|
| CMRRF de Kerpape - 56270 - Ploemeur - Bretagne - France | Marie-Caroline Delebecque, CRA | Contact (sur clinicalTrials) | |||
Critères
Tous
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
- 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
- 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