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Clinical Trial 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.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05108506
Study type Interventional
Source Johns Hopkins University
Contact
Status Completed
Phase N/A
Start date December 5, 2022
Completion date April 1, 2024

See also
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