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Conventional Versus High-Voltage Long-Duration Pulsed Radiofrequency of the Pudendal Nerve

StatusRecruiting
PhaseNot applicable
Started
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Record History

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  1. Primary endpoint revised
    • Eligibility criteria revised
    • Secondary endpoints: details revised at 1 of 4 entries
    v2
  2. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
This study is a single-center, prospective, randomized controlled trial evaluating two types of pulsed radiofrequency (PRF) treatment for patients with pudendal neuralgia. Pudendal neuralgia is a chronic neuropathic pain affecting the perineum and pelvic area, often causing significant discomfort and reduced quality of life. Patients will be randomly assigned to receive either conventional PRF or high-voltage long-duration PRF applied to the pudendal nerve. The study aims to compare the clinical effectiveness, pain relief, and safety of the two treatment approaches. Participants will be monitored for pain improvement, functional outcomes, and any treatment-related side effects. The study follows standard clinical procedures and all treatments are performed under sterile conditions with proper monitoring to ensure patient safety.
Trial Details
NCT Number NCT07356102
Lead Sponsor Ankara City Hospital Bilkent
Conditions
(from sponsor)		 Pudendal Neuralgia
Related terms Pudendal Neuralgia
Enrollment 38 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov