Condition: Hysterectomy · Sponsor: Medical University of South Carolina
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.
This description comes directly from the study's public registry record.
Haley Nitchie, MHA · 843-792-1869 · nitchie@musc.edu
Always discuss trial participation with your own doctor first.
| Medical University of South Carolina | Charleston, South Carolina, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06039566