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Pessary Experience Study

StatusActive, Not Recruiting
PhaseNot specified
Started
View on ClinicalTrials.gov ↗

Record History

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  1. Enrollment closed, study ongoing Show 4 more changesShow less
    • Primary completion date changed from estimate of Dec 2025 to Jan 23, 2026
    • Eligibility criteria expanded, about 12 words
    • Site details revised
    • Publications: details revised at 3 of 3 entries
  2. Primary completion date: Dec 2024 to Dec 2025
    • Study completion date: Dec 2024 to Dec 2026
    • Study description shortened, about 4 words
    v2
  3. 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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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.
Pessaries are silicone devices inserted into the vagina for treatment of pelvic organ prolapse or stress urinary incontinence. They are adequate treatment options for patients who are poor surgical candidates, those who decline surgical intervention, or as a temporizing measure in those ultimately planning surgery. Most studies suggest that about 75% of patients are able to be successfully fit with a pessary, but about 50% discontinue pessary use within 12 months of initiation. The purpose of this study is to determine why pessaries are discontinued.
Trial Details
NCT Number NCT06021769
Lead Sponsor University of Virginia
Conditions
(from sponsor)		 Pelvic Organ Prolapse, Stress Urinary Incontinence
Related terms Pelvic Organ Prolapse, Urinary Incontinence, Stress
Enrollment 30 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov