Peripheral Neuropathy Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- You have been diagnosed with Complex Regional Pain Syndrome (CRPS) affecting one of your arms, along with nerve-related pain
- Your CRPS diagnosis was made using a recognised set of medical guidelines called the Budapest criteria (confirm with trial site)
- Your nerve pain was assessed using a specific questionnaire called the DN4 (confirm with trial site)
- Your CRPS has been present for more than 3 months
- You have no blood clots in the veins or open wounds on your arms
- You are willing to give your consent to take part in the study
- Your medication has not been changed in the last month
- You are covered by a social security or health insurance scheme (this appears to relate to French healthcare — confirm with trial site)
Who may not be able to join:
- You are under a legal guardianship or court-appointed protection order
- You have a mental health condition that affects your ability to give informed consent
- You have severe memory or thinking difficulties that prevent you from accurately describing your pain
- You have a skin condition that would prevent you from wearing a compression sleeve
- You have worn a compression garment before
- You have a history of blood vessel problems, lymph node removal, or any other condition in your arms that can cause swelling, unrelated to CRPS
- You have a known allergy to any ingredient used in Cerecare brand compression garments
- You are pregnant, breastfeeding, or are a woman who could become pregnant and is not using contraception
- You are unable to put the compression garment on by yourself
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Vincent Detaille, Doctor, CMRRF de Kerpape
Phone: 02 97 82 60 28
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
The evolution of pain through Visual Analog Scale (VAS), measured every week for 3 months in the last 24 hours and in the last 7 days
Can't join this trial?
Data last synced from ClinicalTrials.gov: 23 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.