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

Postoperative Nausea and Vomiting Clinical Trial

Official title:
Famotidine Versus Placebo in Emergency Pediatric Surgery as a Risk to Postoperative Nausea and Vomiting ꞉ A Comparative Study by Gastric Ultrasound Measurement

Clinical Trial 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.

Clinical Trial Description

Gastric ultrasound examinations will be performed preoperatively and postoperatively on patients undergoing emergency surgery in pediatric. Gastric cross-sectional area (CSA) will be measured, in order to estimate the gastric volume. The data that will be obtained will be used to evaluate a difference of the gastric volume between the two groups preoperatively and postoperatively and the possible relationship between the gastric volume difference and postoperative adverse event (PONV). ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06211088
Study type Interventional
Source Aswan University Hospital
Contact
Status Active, not recruiting
Phase N/A
Start date January 1, 2023
Completion date June 30, 2024
View Details
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