Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2026-03-26 @ 3:20 PM
Ignite Modification Date:
2026-03-26 @ 3:20 PM
NCT ID:
NCT07356102
Eligibility Criteria:
Inclusion Criteria
* Adults aged 18 years or older
* Diagnosis of pudendal neuralgia according to the Nantes diagnostic criteria
* Followed at the Algology (Pain Medicine) outpatient clinic
* Chronic pudendal neuralgia refractory to conservative treatment or intolerance to conservative therapies
* Not using neuropathic pain medications, or on a stable dose for at least 3 months prior to enrollment
* Ability to comply with study procedures and follow-up visits
* Ability to understand the study information and provide written informed consent
Exclusion Criteria
* Presence of pelvic organic pathologies that may cause pudendal pain
* Pain limited only to the coccygeal, gluteal, or lower abdominal regions
* Patients with purely paroxysmal pain, isolated pruritus, or imaging findings that fully explain symptoms
* History of malignancy or autoimmune disease
* Previous surgery that may have altered the anatomy of the pudendal nerve region
* Pregnancy or suspected pregnancy
* Presence of a cardiac pacemaker or implanted electrical device
* Use of anticoagulant therapy or presence of uncorrectable coagulation disorders
* Active systemic infection or infection at the injection site
* Known hypersensitivity to metals
* Inability or unwillingness to provide informed consent
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT07356102
Study Brief:
Protocol Section:
NCT07356102