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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


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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