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:
- Adults aged 18 years or older
- People who have been diagnosed with pudendal neuralgia using a specific set of recognised diagnostic guidelines called the Nantes criteria
- People who are currently being seen at a Pain Medicine outpatient clinic
- People whose pudendal neuralgia has been long-lasting and has not responded to standard treatments, or who cannot tolerate those treatments
- People who are either not taking any medications for nerve pain, or who have been on a steady, unchanged dose of such medications for at least 3 months before joining
- People who are able to attend all required study appointments and follow through with the study procedures
- People who are able to understand the study information and agree in writing to take part
Who may not be able to join:
- People who have a physical condition in the pelvic area that could be causing the pudendal pain (other than nerve-related causes)
- People whose pain is only felt in the tailbone, buttock, or lower abdominal areas
- People whose pain occurs only in sudden, brief bursts, or who have only itching, or whose medical scans fully account for all their symptoms
- People with a personal history of cancer or an autoimmune disease
- People who have had surgery in the past that may have changed the structure of the area around the pudendal nerve
- People who are pregnant or who may be pregnant
- People who have a cardiac pacemaker or any other implanted electrical device in their body
- People who are taking blood-thinning medications or who have a clotting disorder that cannot be corrected
- People who have an active infection anywhere in the body, or an infection at the site where the procedure would be performed
- People with a known allergy or sensitivity to metals
- People who are unable or unwilling to provide written consent to participate
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: +905333316636
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 Intensity Assessed by Numeric Rating Scale (NRS)
Can't join this trial?
Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.