Pain with Differing Intraperitoneal Washes At the End of Laparoscopic Gynecologic Surgery
Starting soon · Phase 4
Conditions studied: Laparoscopic Adnexal Surgery
In brief
We hypothesize that instilling intraperitoneal Marcaine (without epinephrine) at the end of a non-total laparoscopic gynecologic surgery (adnexa only, which includes the ovaries, fallopian tubes, and associated ligaments, vessels, and connective tissue) will result in less pain and reduced opioid use postoperatively.
Key facts
- Study ID
- NCT06842771
- Run by
- University of Tennessee
- People needed
- 96
- Starts
- 2025-03-01
- Expected to finish
- 2027-03-01
- Last updated by the study team
- 2025-02-24
Who can join
Age: 18 and older. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- Age 18 years and older
- Undergoing planned laparoscopic adnexal surgery as a day surgery procedure; The surgical site is the "adnexa" which contains the ovaries, fallopian tubes, and associated ligaments, vessels, and connective tissue. The "adnexa" does not include the uterus.
- BMI 55.0 or less
You may not qualify if…
- Under age 18
- Undergoing a non-laparoscopic unplanned surgical procedure Patients having a laparoscopic partial or complete removal of the uterus, a hysterectomy, will NOT be included in this study population for enrollment.
- septicemia
- severe hemorrhage
- severe hypotension or shock
- arrhythmias
- known hypersensitivity to bupivacaine or to any other local anesthetic agent
- local infection at the injection site
Where it is running
- University of Tennessee Health Science Center — Memphis, Tennessee, United States
Full record on ClinicalTrials.gov
Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.