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Synthetic Versus Autologous Sling For Stress Incontinence

Study acronym: SASSI
StatusRecruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗

Record History

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  1. Trial sites expanded: 1 → 7 locations
    • Eligibility criteria expanded, about 21 words
  2. Trial status: Not Yet Recruiting to Recruiting
    • Start date changed from estimate of Jan 2026 to Jan 12, 2026
    v4
  3. Start date: Jan 2032 to Jan 2026
    • Study title shortened, about 1 word
    v3
  4. Re-verified, no change to tracked fieldsv2
  5. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
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.
Trial Details
NCT Number NCT07276295
Lead Sponsor University of British Columbia
Collaborators: Canadian Institutes of Health Research (CIHR)
Conditions
(from sponsor)		 Urinary Incontinence
Related terms Urinary Incontinence
Enrollment 232 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov