RecruitingNot ApplicableNCT07511491

Ondansetron Lozenge Versus Intravenous for Prevention of Shivering in Cesarean Section

Effect of Ondansetron Lozenge Versus Intravenous for Prevention of Shivering in Cesarean Section: A Randomized Controlled Trial


Sponsor

Tanta University

Enrollment

90 participants

Start Date

Apr 11, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

This study aims to compare the effect of ondansetron lozenge and intravenous for prevention of shivering in cesarean section (CS).


Eligibility

Sex: FEMALEMin Age: 18 YearsMax Age: 40 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called Ondansetron intravenous and a drug called Ondansetron lozenge for people with cesarean section, intravenous, and other related conditions. The study is currently recruiting participants at 1 location. People eligible for this study include women aged 18 Years to 40 Years.

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

DRUGOndansetron lozenge

Patients will receive ondansetron lozenge 4 mg (Ondalenz ©), 2 hours before surgery.

DRUGOndansetron intravenous

Patients will receive 8 mg of ondansetron IV just before the surgery.


Locations(1)

Tanta University

Tanta, El-Gharbia, Egypt

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NCT07511491


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