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NCT05108506 · ClinicalTrials.gov registry record · NA
Strict Need to Void After Same-day Discharge, Non-urogynecologic, Minimally Invasive Hysterectomy
A NA study of Urinary Retention Postoperative, sponsored by Johns Hopkins University.
- Completed
- Registry status
- NA
- Development phase
- 205
- Enrollment target
- 1
- Study location
NCT05108506 is a NA study of Urinary Retention Postoperative that has completed, run by Johns Hopkins University. The registered enrollment target is 205 participants, below the 23,391-participant average among 3 other Urinary Retention Postoperative trials with a reported enrollment target (99% lower). The trial reports 1 study location across 1 state.
The verdict
NCT05108506, a NA study of Urinary Retention Postoperative, has completed, sponsored by Johns Hopkins University.
- COMPLETED
- Registry status
- NA
- Development phase
- 205 participants
- Enrollment target
- 1
- Study location
Study Summary
Patients who are undergoing non-urogynecologic, minimally invasive (laparoscopic, robotic) hysterectomy who are discharged the day of surgery will be randomized to a strict need to void versus no need to void prior to discharge. To determine if a strict versus liberal voiding trial following the aforementioned surgery in same day discharge patients increases rates of post-operative urinary retention, urinary tract infection (UTI), or re-presentation and if there is a difference in Post-Anesthesia Care Unit (PACU) time and costs.
Conditions Studied
Interventions
- BEHAVIORAL No Strict need to void following surgery
- BEHAVIORAL Strict need to void following surgery
Study Locations (1)
Maryland
- Johns Hopkins Hospital - Baltimore
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 205 participants |
| Start Date | 2022-12-05 |
| Est. Completion | 2024-04-01 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT05108506
The ClinicalTrials.gov registry entry for NCT05108506 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 205 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 23,391-participant average among 3 other Urinary Retention Postoperative trials with a reported enrollment target (99% lower). The listed sponsor is Johns Hopkins University, which has 1,448 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Urinary Retention Postoperative appearing as the primary indexed condition, and to 2 interventions - of which No Strict need to void following surgery is the first listed.
NCT05108506 reports 1 study location spanning 1 distinct geographic area - top geographies include Maryland.
Frequently Asked Questions
What is clinical trial NCT05108506 about?
NCT05108506 is a clinical study titled "Strict Need to Void After Same-day Discharge, Non-urogynecologic, Minimally Invasive Hysterectomy". Patients who are undergoing non-urogynecologic, minimally invasive (laparoscopic, robotic) hysterectomy who are discharged the day of surgery will be randomized to a strict need to void versus no need to void prior to discharge. To determine if a strict versus liberal voiding trial following the af...
What is the current status of trial NCT05108506?
This trial is currently completed. It is a NA study. The enrollment target is 205 participants. The study started on 2022-12-05. Estimated completion is 2024-04-01.
What conditions does trial NCT05108506 study?
This clinical trial studies the following conditions: Urinary Retention Postoperative.
What interventions are being tested in trial NCT05108506?
The interventions under investigation include: No Strict need to void following surgery (BEHAVIORAL), Strict need to void following surgery (BEHAVIORAL).
Who is sponsoring clinical trial NCT05108506?
This trial is sponsored by Johns Hopkins University, which has 1,448 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT05108506 being conducted?
This trial has 1 study location across Maryland. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Read our methodology - how this data is sourced, computed, and verified.
Related
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