At a glance
ClinicalIndex Comparison RecordN/ACompleted· 58 enrolled
Drug / intervention
Preoperative Pessary Usedevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Prediction of Postsurgical Symptomatic Outcomes With Preoperative Pessary Use
In Brief
A clinical study evaluating Preoperative Pessary Use for Vaginal Vault Prolapse and 3 related conditions. Completed, enrolled 58 participants across 1 site.
Detailed Summary
This is a single center, prospective trial of pessary use prior to reconstructive pelvic floor surgery for pelvic organ prolapse. The goal of the study is to evaluate the change in pelvic floor symptoms with pessary use and subsequent reconstructive surgery. Additionally, we will assess the impact that preoperative pessary use has on patient self-reported preparedness for surgery.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
20162017201820192020202120222023202420252026
First PostedFeb 2016
Enrollment StartMar 2016
Primary CompletionOct 2019
Study CompletionDec 2019
TodayJul 2026
First PostedFeb 11, 2016
Enrollment StartMar 11, 2016
Primary CompletionOct 31, 2019
Study CompletionDec 31, 2019
TodayJul 2, 2026
Enrollment to primary: 3.6 yearsPosted 10.4 years ago
Interventions
Preoperative Pessary Usedevice
Pessary use for 1-4 weeks prior to surgical prolapse repair