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Pessary Experience Study

NCT06021769 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 30

Last updated 2025-01-28

No results posted yet for this study

Summary

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.

Conditions

  • Pelvic Organ Prolapse
  • Stress Urinary Incontinence

Interventions

OTHER

Observational only

No intervention

Sponsors & Collaborators

  • University of Virginia

    lead OTHER

Principal Investigators

  • Monique Vaughan, MD · Assistant Professor

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2023-06-12
Primary Completion
2025-12-31
Completion
2026-12-31

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06021769 on ClinicalTrials.gov