Trials / Completed
CompletedNCT07030647
"Efficacy of Local Anesthetic for Postoperative Pain in Gynecologic Laparoscopy"
Efficacy of the Analgesic Effect of Local Anesthetic Injection on Postoperative Pain in Gynecological Laparoscopic Surgeries: A Randomized Controlled Trial
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 90 (actual)
- Sponsor
- Usama Ahmed Elsaeed Salem, MD · Academic / Other
- Sex
- Female
- Age
- 18 Years – 60 Years
- Healthy volunteers
- Not accepted
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.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Bupivacaine 0.25% | At the end of gynecologic laparoscopic surgery and prior to trocar removal, 40 mL of Bupivacaine 0.25% is instilled intraperitoneal under direct vision to evaluate its analgesic effect. |
| DRUG | Bupivacaine 0.25% | Before trocar insertion in gynecologic laparoscopic surgery, 5 mL of Bupivacaine 0.25% is infiltrated subcutaneously at each trocar port site to assess its effect on postoperative pain. |
Timeline
- Start date
- 2024-03-01
- Primary completion
- 2025-02-05
- Completion
- 2025-03-30
- First posted
- 2025-06-22
- Last updated
- 2025-06-22
Locations
1 site across 1 country: Egypt
Source: ClinicalTrials.gov record NCT07030647. Inclusion in this directory is not an endorsement.