Hybrid Transobturator Tape Versus Conventional Synthetic Tape for Stress Urinary Incontinence (NCT07762300) | Clinical Trial Compass
RecruitingNot Applicable
Hybrid Transobturator Tape Versus Conventional Synthetic Tape for Stress Urinary Incontinence
Egypt90 participantsStarted 2026-07-01
Plain-language summary
This randomized controlled trial compares the safety, efficacy, and impact on female sexual function of a novel hybrid transobturator tape (combining an autologous rectus fascia strip with a polypropylene mesh) versus standard synthetic transobturator tape in women undergoing surgery for stress urinary incontinence.
Who can participate
Age range
18 Years
Sex
FEMALE
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:
* Female patients suffering from genuine stress urinary incontinence.
* Failed conservative management (pelvic floor exercises, medical therapy)
* Written informed consent.
Exclusion Criteria:
* Mixed urinary incontinence with predominant urge component.
* High-grade pelvic organ prolapse (POP-Q Stage \>= II), which required surgical intervention.
* Neurogenic bladder or voiding dysfunction (Post-void residual \> 100 ml).
* Coagulopathy or active urinary tract infection.
* Patients who underwent recent pelvic radiotherapy.
* Previous incontinence surgery (recurrent cases).
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
1
Incidence of mesh-related complications (including vaginal erosion, extrusion, and chronic groin pain).