Intraperitoneal Bupivacaine for Pelvic Organ Prolapse

Status Recruiting

Clinical Trial Summary

The purpose of this study is to evaluate the effects of 30 mL intraperitoneal Bupivacaine without epinephrine 0.25% on postoperative pain control in patients undergoing pelvic organ prolapse repair. The investigators hypothesize that use of intraperitoneal Bupivacaine will decrease postoperative pain scores and opiate consumption in the postoperative period, following pelvic organ prolapse repair.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT06120530
Study type	Interventional
Source	Indiana University
Contact	Jose J Lazaro Weiss, MD
Phone	7274241947
Email	jlazarow@iu.edu
Status	Recruiting
Phase	Phase 4
Start date	August 15, 2023
Completion date	January 1, 2025

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See also
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