The Role of Sugammadex in Posotoperative Urinary Retention in Patients Undergoing Pelvic Floor Reconstructive Procedures

Postoperative Urinary Retention Clinical Trial

Official title:
A Randomized Clinical Trial to Determine the Effect of Transient Postoperative Urinary Retention Using Sugammadex (4 mg x kg) Versus Glycopyrrolate and Neostigmine (0.01 mg/kg - 50mg/kg) in Patients Undergoing Vaginal Hysterectomies With and Without Pelvic Organ Prolapse Procedures: A Pilot Study

Status Recruiting

Clinical Trial Summary

The Investigator will perform a single-institution randomized double-blinded controlled trial comparing intraoperative Sugammadex vs. standard dose of glycopyrrolate/neostigmine combination for participants undergoing a total vaginal hysterectomy with or without pelvic organ prolapse procedures under general endotracheal anesthesia.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT05664633
Study type	Interventional
Source	West Virginia University
Contact	Omar Duenas Garcia, MD
Phone	855-WVU-CARE
Email	omar.duenasgarcia@hsc.wvu.edu
Status	Recruiting
Phase	Phase 1/Phase 2
Start date	August 2023
Completion date	June 2024

View Details

See also
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