CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 158 enrolled
Drug / intervention
Self-removalprocedure
Likely dose
Not stated in record
Key inclusion· 3
  • Undergoing vaginal vault suspension or robot-assisted laparoscopic sacrocolpopexy for pelvic organ prolapse treatment
  • Failed voiding trial prior to discharge
  • May have concomitant procedures including hysterectomy, suburethral sling, anterior/posterior colporrhaphy, bilateral salpingectomy or salpingooophorectomy
Key exclusion· 2
  • Physical or mental impairment affecting ability to self-remove catheter (e.g., Multiple Sclerosis, Dementia, Parkinsonism, impaired mobility, wheelchair-bound)
  • Bladder injury, fistula repair, or other conditions requiring prolonged catheterization

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02996968
NCT02996968N/ACompleted

Is Self-discontinuation of a Transurethral Catheter Following Pelvic Reconstructive Surgery as Effective as Office-based Discontinuation?; A Randomized Controlled Trial

TriHealth Inc.·interventional·Posted Dec 19, 2016·Updated Nov 12, 2019

In Brief

A clinical study evaluating Self-removal for Postoperative Urinary Retention. Completed, enrolled 158 participants across 1 site.

Detailed Summary

This study is to determine if self-discontinuation of transurethral foley catheters in patients diagnosed with postoperative urinary retention (POUR), which is defined as the continued need for catheterization, following impatient pelvic organ prolapse surgery is non-inferior to office-discontinuation.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

N/ACompletedFinished
2017201820192020202120222023202420252026
First PostedDec 19, 2016
Enrollment StartJan 10, 2017
Primary CompletionMay 16, 2019
TodayJul 2, 2026
Enrollment to primary: 2.4 yearsPosted 9.5 years ago

Interventions

Self-removalprocedure

Self-discontinuation of a transurethral catheter