Timing of Active Void Trials After Urogynecologic Procedures

Status Recruiting

Clinical Trial Summary

The goal of this clinical trial is to learn about active void trial pass rates in patients undergoing urogynecologic surgery. The main question it aims to answer is the comparison in pass rate during active void trial between women who are given 30 minutes versus 60 minutes to void following urogynecologic surgery. Patient will be randomized to two arms prior to scheduled surgery. During the active void trial, women will be allotted up to 30 minutes or up to 60 minutes to void depending on respective randomization.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT05885958
Study type	Interventional
Source	University of South Florida
Contact	Simone Fertel, MD
Phone	5049313383
Email	sfertel@usf.edu
Status	Recruiting
Phase	N/A
Start date	July 3, 2023
Completion date	June 2025

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