RecruitingPhase 4NCT07190495

Ginger to Prevent Nausea and Vomiting After Laparoscopic Cholecystectomy

Preoperative Ginger for the Prevention of Postoperative Nausea and Vomiting in Patients Undergoing Laparoscopic Cholecystectomy: A Double-Blind Randomized Controlled Trial


Sponsor

University Tunis El Manar

Enrollment

102 participants

Start Date

Jul 5, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

This study aims to evaluate whether preoperative oral administration of ginger (800 mg, given 2 hours before surgery) reduces the incidence and severity of postoperative nausea and vomiting (PONV) within the first 24 hours after laparoscopic cholecystectomy.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called Ginger and a drug called Placebo for people with laparoscopic cholecystectomy and postoperative nausea and vomiting. The study is currently recruiting participants at 1 location. People eligible for this study include aged 18 Years and older.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGGinger

Patients will receive 800 mg of oral ginger 2 hours before laparoscopic cholecystectomy

DRUGPlacebo

Patients will receive an oral placebo capsule identical in appearance to ginger, administered 2 hours before laparoscopic cholecystectomy


Locations(1)

Mohamed Taher Maamouri University Hospital

Nabeul, Nabeul Governorate, Tunisia

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NCT07190495


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