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Recruiting NCT05034835

NCT05034835 Impact of Compression Garments on Pain in Patients With Complex Regional Pain Syndrome of the Upper Limbs.

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Clinical Trial Summary
NCT ID NCT05034835
Status Recruiting
Phase
Sponsor Centre Mutualiste de Rééducation et de Réadaptation Fonctionnelles de Kerpape
Condition Complex Regional Pain Syndromes
Study Type INTERVENTIONAL
Enrollment 60 participants
Start Date 2021-10-12
Primary Completion 2026-05

Trial Parameters

Condition Complex Regional Pain Syndromes
Sponsor Centre Mutualiste de Rééducation et de Réadaptation Fonctionnelles de Kerpape
Study Type INTERVENTIONAL
Phase N/A
Enrollment 60
Sex ALL
Min Age 18 Years
Max Age N/A
Start Date 2021-10-12
Completion 2026-05
Interventions
usual treatment with compression garments (CERECARE)usual treatment without compression garments (CERECARE)

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Brief Summary

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.

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 t

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