"Efficacy of Local Anesthetic for Postoperative Pain in Gynecologic Laparoscopy"
Status:
COMPLETED
Trial end date:
2025-03-30
Target enrollment:
Participant gender:
Summary
This is a randomized, double-blind, controlled clinical trial evaluating the efficacy of local anesthetic (LA) in reducing postoperative pain in patients undergoing gynecologic laparoscopic surgery. Ninety participants will be randomly assigned into three equal groups: Group A will receive LA injection at the port site, Group B will receive intraperitoneal LA injection, and Group C will serve as the control group with no LA intervention. Postoperative pain will be assessed and compared among the three groups.