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Ginger to Prevent Nausea and Vomiting After Laparoscopic Cholecystectomy (GINGER-PONV)

U

University Tunis El Manar

Status and phase

Enrolling
Phase 4

Conditions

Laparoscopic Cholecystectomy
Postoperative Nausea and Vomiting

Treatments

Drug: Ginger
Drug: Placebo

Study type

Interventional

Funder types

Other

Identifiers

NCT07190495
GINGER PONV

Details and patient eligibility

About

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.

Enrollment

102 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age ≥ 18 years.
  • Scheduled for elective laparoscopic cholecystectomy under general anesthesia.
  • American Society of Anesthesiologists (ASA) physical status I-III.
  • Able to understand the study procedures and provide written informed consent.

Exclusion criteria

  • Known allergy or hypersensitivity to ginger
  • Documented history of bleeding disorders or current treatment with anticoagulant agents
  • History of severe postoperative nausea and vomiting or an Apfel score of 4
  • Administration of antiemetic drugs or corticosteroids during the preoperative period
  • Pregnancy or breastfeeding
  • Active gastrointestinal or liver disease

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

102 participants in 2 patient groups, including a placebo group

Ginger group
Active Comparator group
Description:
Patients will receive 800 mg of oral ginger 2 hours before laparoscopic cholecystectomy
Treatment:
Drug: Ginger
Placebo group
Placebo Comparator group
Description:
Patients will receive an oral placebo capsule identical in appearance to ginger, administered 2 hours before laparoscopic cholecystectomy
Treatment:
Drug: Placebo

Trial contacts and locations

1

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Central trial contact

Ibtissem BEN TALEB, M.D.

Data sourced from clinicaltrials.gov

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