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:
- People who have had shingles and are still experiencing persistent nerve pain along the same area of skin for at least 90 days after the shingles outbreak
- People aged 18 years or older, of any gender
- People who are willing to follow the study procedures and attend all required follow-up appointments
- People who are able and willing to sign a written consent form agreeing to take part
Who may not be able to join:
- People who have had an allergic reaction to any of the treatments being used in this study
- People who are pregnant
- People who have any type of skin infection in the area affected by their shingles pain
- People whose immune system is weakened, including those with cancer or HIV
- People who have a condition called bone marrow aplasia, which affects the body's ability to produce blood cells
- People who have a known tendency to bleed easily, problems with how their blood clots, or a low platelet count (below a certain level in a blood test)
- People who regularly take blood-thinning or anti-clotting medications
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
Phone: +201067070550
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
Change in Pain Severity Using the Visual Analog Scale
Can't join this trial?
Data last synced from ClinicalTrials.gov: 9 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.