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NCT05885958 · ClinicalTrials.gov registry record · NA
Timing of Active Void Trials After Urogynecologic Procedures
A NA study of Postoperative Care and Urogynecology, sponsored by University of South Florida.
- Completed
- Registry status
- NA
- Development phase
- 231
- Enrollment target
- 1
- Study location
NCT05885958 is a NA study of Postoperative Care and Urogynecology that has completed, run by University of South Florida. The registered enrollment target is 231 participants, above the 90-participant average among 4 other Postoperative Care trials with a reported enrollment target (157% higher). The trial reports 1 study location across 1 state.
The verdict
NCT05885958, a NA study of Postoperative Care and Urogynecology, has completed, sponsored by University of South Florida.
- COMPLETED
- Registry status
- NA
- Development phase
- 231 participants
- Enrollment target
- 1
- Study location
Study 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 Studied
Interventions
- OTHER Time
Study Locations (1)
Florida
- USF Urogynecology Clinic - Tampa
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 231 participants |
| Start Date | 2023-07-03 |
| Est. Completion | 2025-06-05 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT05885958
The ClinicalTrials.gov registry entry for NCT05885958 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 231 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 90-participant average among 4 other Postoperative Care trials with a reported enrollment target (157% higher). The listed sponsor is University of South Florida, which has 252 total studies on file at ClinicalTrials.gov.
The record links to 3 conditions, with Postoperative Care appearing as the primary indexed condition, and to 1 intervention - of which Time is the first listed.
NCT05885958 reports 1 study location spanning 1 distinct geographic area - top geographies include Florida.
Frequently Asked Questions
What is clinical trial NCT05885958 about?
NCT05885958 is a clinical study titled "Timing of Active Void Trials After Urogynecologic Procedures". 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 urogyne...
What is the current status of trial NCT05885958?
This trial is currently completed. It is a NA study. The enrollment target is 231 participants. The study started on 2023-07-03. Estimated completion is 2025-06-05.
What conditions does trial NCT05885958 study?
This clinical trial studies the following conditions: Postoperative Care, Urogynecology, Urinary Catheters.
What interventions are being tested in trial NCT05885958?
The interventions under investigation include: Time (OTHER).
Who is sponsoring clinical trial NCT05885958?
This trial is sponsored by University of South Florida, which has 252 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT05885958 being conducted?
This trial has 1 study location across Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Related
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