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Clinical Trial Summary

This study will enroll females who are ages 18 and older undergoing a laparoscopic or robotic, partial or full hysterectomy. Participants will be randomized to receive IV n-acetylcysteine or placebo during the first 60 minutes of their procedure. At various time points after the procedure patients will be asked to report their pain scores, and any pain medication taken.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06039566
Study type Interventional
Source Medical University of South Carolina
Contact Haley Nitchie, MHA
Phone 843-792-1869
Email nitchie@musc.edu
Status Recruiting
Phase Phase 3
Start date November 30, 2023
Completion date October 9, 2025

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