Clinical Trials Directory

Trials / Completed

CompletedNCT05885958

Timing of Active Void Trials After Urogynecologic Procedures

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
231 (actual)
Sponsor
University of South Florida · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Not accepted

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.

Conditions

Interventions

TypeNameDescription
OTHERTimePatients will be given up to 30 minutes to void.
OTHERTimePatients will be given up to 60 minutes to void.

Timeline

Start date
2023-07-03
Primary completion
2024-08-27
Completion
2025-06-05
First posted
2023-06-02
Last updated
2025-07-01

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT05885958. Inclusion in this directory is not an endorsement.

Timing of Active Void Trials After Urogynecologic Procedures (NCT05885958) · Clinical Trials Directory