drugset / Trial / NCT07030647
"Efficacy of Local Anesthetic for Postoperative Pain in Gynecologic Laparoscopy"
RandomizedParallel-groupDouble-blindTreatment
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.
Timeline
- Start
- 2024-03-01
- Primary completion
- 2025-02-05
- Completion
- 2025-03-30
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Bupivacaine | Other / unclassified | 0.25 % | Other |
Indications
No indication recorded.