CompletedNot Applicable

A PSM Analysis to Evaluate Electrical Pudendal Nerve Stimulation for PPI

China389 participantsStarted 2023-12-01

Plain-language summary

The goal of this propensity score matching study is to compare the posttreatment outcomes of post-radical prostatectomy Incontinence patients undergoing either electrical pudendal nerve stimulation or pelvic floor muscle training combined with transanal electrical stimulation.

Who can participate

Age range

18 Years – 80 Years

Sex

MALE

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Onset of urinary incontinence at least 1 month post-RP * Minimum two documented incontinence episodes per week in a 7-day bladder diary * Pathological confirmation of no residual cancer post-RP Exclusion Criteria: * High pathological risk factors (e.g., lymph node metastasis, resection margin involvement, bulky tumors) * Preoperative incontinence * Prior anticholinergic treatment * Urinary tract infection or hematuria * Postvoid residual volume exceeding 100 ml (determined by bladder ultrasound) * Neurological disorders * Urethral stricture

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

International Consultation on Incontinence Questionnaire-short form score (ICIQ-SF)

Timeframe: T0 (baseline); T1 (day after 24th treatment); T2 (day after 36th treatment); T3 (day after 48th treatment); T4 (day after 60th treatment); T5 (day after 72nd treatment).

Trial details

NCT IDNCT06130306

SponsorShanghai Institute of Acupuncture, Moxibustion and Meridian

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2024-11-30

View on ClinicalTrials.gov More Urinary Incontinence Following Surgical Procedure trials