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Study identifier: NCT07276295 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Synthetic Versus Autologous Sling For Stress Incontinence

Condition: Urinary Incontinence  ·  Sponsor: University of British Columbia

PhaseNA
Planned participants232
Who can joinFemale, 60 Years to no upper limit
Healthy volunteersNo

About this study

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 investigation of opioid use, mental health, sexual health, and other post-op outcomes.

This description comes directly from the study's public registry record.

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Locations (1)

St. Paul's HospitalVancouver, British Columbia, CanadaRecruiting

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Source record: clinicaltrials.gov/study/NCT07276295