Synthetic Versus Autologous Sling For Stress Incontinence
Recruiting
N/A
Interventional Study
Urinary Incontinence
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 60 and older
- Sex
- Female
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 232 (estimated)
- Sponsor
- University of British Columbia · Other
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About This Trial
This is a multi-centre randomized controlled trial comparing mid-urethral synthetic mesh sling or tension-free vaginal tape (TVT) and autologous fascia sling (AFS) in elderly patients with stress predominant urinary incontinence. The investigators aim to investigate new onset pelvic pain 6 months post-op and objective urinary incontinence cure rate 5 years post-op. Secondary objectives include inv…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Adult females at birth (female anatomy, any gender)
* Greater than or equal to 60 years old
* Have stress predominant urinary incontinence (spUI) eligible for both types of surgery (tension-free vaginal tape and autologous fascia sling)
* Exhausted conservative management opti…
Contacts
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