drugset / Trial / NCT06211088

Famotidine Versus Placebo in Emergency Pediatric Surgery As a Risk to Postoperative Nausea and Vomiting

NCT06211088

Completed 50 enrolled Aswan University Hospital
RandomizedParallel-groupDouble-blindOther

Summary

The aim of this study is to evaluate the difference of the gastric volume by quantitative measurements of gastric antrum preoperatively and postoperatively by using 5mg famotidine versus placebo as a risk factor of PONV.

Timeline

Start
2024-08-01
Primary completion
2024-12-30
Completion
2025-01-30

Drugs

EvaluationDrugModalityDoseRoute
Comparator Famotidine Other / unclassified 5 mg

Indications

No indication recorded.