About this trial
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.
Eligibility criteria
Qualifiers
English-speaking women aged 18 years or older
Choosing to undergo a pessary fitting for symptomatic pelvic organ prolapse and/or stress urinary incontinence at the University of Virginia Pelvic Medicine and Reconstructive Surgery clinic
Willingness and ability to comply with scheduled visits and study procedures.
Successful pessary fitting
Disqualifiers
Pregnant women
Prisoners
Cognitively impaired
Non-English speaking subjects
Trial design
Treatments tested in this trial
- Observational only