Phase
Condition
Reflex Sympathetic Dystrophy Syndrome (Rsds)
Mood Disorders
Somatoform And Dissociative Disorders
Treatment
usual treatment with compression garments (CERECARE)
usual treatment without compression garments (CERECARE)
Clinical Study ID
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
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
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 anyother pathology that can lead to edema regardless of CRPS
Known allergy to one of the components of the compression garments of the Cerecarebrand
Declared pregnancy, breastfeeding woman or woman of childbearing potential withoutcontraception
Inability to put on the compression garment alone
Study Design
Connect with a study center
CMRRF de Kerpape
Ploemeur, Bretagne 56270
FranceSite Not Available
CMRRF de Kerpape
Ploemeur 2986732, Brittany Region 3030293 56270
FranceActive - Recruiting

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