Viewing Study NCT05108506



Ignite Creation Date: 2024-05-06 @ 4:50 PM
Last Modification Date: 2024-10-26 @ 2:17 PM
Study NCT ID: NCT05108506
Status: COMPLETED
Last Update Posted: 2024-04-17
First Post: 2021-10-25

Brief Title: Strict Need to Void After Same-day Discharge Non-urogynecologic Minimally Invasive Hysterectomy
Sponsor: Johns Hopkins University
Organization: Johns Hopkins University

Study Overview

Official Title: To Void or Not to Void After Same-day Discharge Non-urogynecologic Minimally Invasive Hysterectomy That is the Question
Status: COMPLETED
Status Verified Date: 2024-07
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief 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
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None