Clinical trial Recruiting at 1 site Interventional Ages 18 to 80 Men only

Using magnetic stimulation and pelvic exercises to treat urinary incontinence after prostate surgery

Official title: Efficacy of Extracorporeal Magnetic Stimulation, Pelvic Floor Muscle Exercise, and Combination of Both in Management of Post Radical Prostatectomy Urinary Incontinence: A Randomized Controlled Trial

Run by Hamad General Hospital · NCT05680168 · Data updated 2026-11-12

This study is testing whether magnetic stimulation, pelvic exercises, or a mix of both can help men with urinary incontinence after prostate surgery feel better.

Quick facts

Study typeInterventional
Ages18 Years to 80 Years
SexMen only
Enrollment60 (estimated)
SponsorHamad General Hospital
Government
Locations1 site (Doha)
StatusRecruiting
StartedJanuary 1, 2023
Main results expectedFebruary 1, 2029
Study endsDecember 31, 2029
Registry record updatedJanuary 13, 2023
Trial IDNCT05680168 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are adult males aged 18 and above with localized low to intermediate risk prostate cancer undergoing radical prostatectomy.

Probably not a fit

Patients with high-risk prostate cancer, those who had prior treatments like chemotherapy or radiotherapy, or those with pre-existing urinary issues will not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study evaluates the effectiveness of extracorporeal magnetic stimulation, pelvic floor muscle exercises, and a combination of both in managing urinary incontinence following radical prostatectomy. Male patients aged 18 and older with localized prostate cancer will be randomized into three groups to receive different treatment modalities. The study aims to determine which approach is most effective in alleviating urinary incontinence symptoms over a period of seven years. Participants will be recruited from the urology department at Hamad General Hospital in Doha.

Why it matters

Potential benefit: If successful, this study could provide a more effective treatment option for men suffering from urinary incontinence after prostate surgery.

How similar studies have gone: Other studies have shown promising results with similar approaches, but this specific combination of treatments is relatively novel.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* The study population will include all adult male patients 18 years of age and above, with localized prostate cancer of low or intermediate risk disease who chose definitive treatment with radical prostatectomy either through open radical retropubic prostatectomy (RRP) or through robotic assissted laparoscopic radical prostatectomy (RALP) as first line for treatment and had the surgery under Hamad General Hospital urology department care.

Exclusion Criteria:

* Patients with high risk , locally advanced or metastatic prostate cancer at time of diagnosis
* Patients with low to intermediate risk prostate cancer who received chemo or radiotherapy then had salvage surgery
* Patients with urinary incontinence or diagnosed overactive bladder before radical prostatectomy.
* Patients with complicated surgery resulting in anastomotic leak, prolonged catheterisation more than 3 weeks, reinsertion of catheter due to retention of urine.
* Patients who refuse to participate in the clinical trial.

Where it's running

  • Ambulatory Care Center
    Doha, Qatar
    Recruiting

Study contacts

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.