[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100517763":3},{"organization":4,"armGroups":7,"interventions":14,"overallOfficials":19,"centralContacts":24,"locations":31,"responsibleParty":45,"collaborators":10,"id":46,"slug":47,"hasResults":48,"nctId":49,"briefTitle":50,"officialTitle":51,"acronym":10,"eligibilityCriteria":52,"healthyVolunteers":53,"sex":54,"minAge":55,"maxAge":10,"enrollmentInfo":56,"targetDuration":10,"studyType":59,"phases":10,"briefSummary":60,"conditions":61,"keywords":64,"overallStatus":33,"whyStopped":10,"lastUpdateSubmitDate":66,"lastUpdatePostDateStruct":67,"startDateStruct":70,"completionDateStruct":72,"leadSponsor":74,"locationsCount":75},{"fullName":5,"class":6},"University of Virginia","OTHER",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"Women being fitted with pessaries",null,"Women being fitted with pessaries as standard of care will be eligible to participate. They will be asked to complete a recorded verbal interview and written questionnaires the day they have their pessaries fitted and at their follow-up clinic appointments at 4-6 weeks, 3 months, 6 months, and 12 months. Another recorded video interview will be completed at the 12 month appointment.",[13],"Other: Observational only",[15],{"type":6,"name":16,"description":17,"armGroupLabels":18,"otherNames":10},"Observational only","No intervention",[9],[20],{"name":21,"affiliation":22,"role":23},"Monique Vaughan, MD","Assistant Professor","PRINCIPAL_INVESTIGATOR",[25,29],{"name":21,"role":26,"phone":27,"phoneExt":10,"email":28},"CONTACT","4349261955","mv4w@UVAHEALTH.ORG",{"name":21,"role":26,"phone":30,"phoneExt":10,"email":28},"4349242103",[32],{"facility":5,"status":33,"city":34,"state":35,"zip":36,"country":37,"countryCode":38,"cosmosGeoPoint":39,"geoPoint":44,"contacts":10},"RECRUITING","Charlottesville","Virginia","22903","United States","US",{"type":40,"coordinates":41},"Point",[42,43],-78.47668,38.02931,{"lat":43,"lon":42},{"type":23,"investigatorFullName":21,"investigatorTitle":22,"investigatorAffiliation":5,"oldNameTitle":10,"oldOrganization":10},"100517763","pessary-experience-study-100517763",false,"NCT06021769","Pessary Experience Study","Longitudinal Assessment of Pessary Experience","Inclusion Criteria:\n\n* English-speaking women aged 18 years or older\n* Choosing to undergo a pessary fitting for symptomatic pelvic organ prolapse and\u002For stress urinary incontinence at the University of Virginia Pelvic Medicine and Reconstructive Surgery clinic\n* Willingness and ability to comply with scheduled visits and study procedures.\n* Successful pessary fitting\n\nExclusion Criteria:\n\n* Pregnant women\n* Prisoners\n* Cognitively impaired\n* Non-English speaking subjects\n* Patients who cannot comply with pessary check visits\n* Active vaginal infection\n* Vaginal malignancy\n* Genitourinary tract fistula",true,"FEMALE","18 Years",{"count":57,"type":58},30,"ESTIMATED","OBSERVATIONAL","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.",[62,63],"Pelvic Organ Prolapse","Stress Urinary Incontinence",[65],"pessary","2025-01-26",{"date":68,"type":69},"2025-01-28","ACTUAL",{"date":71,"type":69},"2023-06-12",{"date":73,"type":58},"2026-12",{"name":5,"class":6},1]