Clinical Trial

Gastric Volume and Fasting Duration in Pregnant Women

Study acronym: PREG-GAS
Completed
View on ClinicalTrials.gov →
Summary
This prospective observational study aimed to evaluate the effect of preoperative fasting duration on gastric volume and antral visibility in pregnant women undergoing elective cesarean section. Patients were divided into two groups according to fasting duration (6-8 hours and 8-10 hours), and preoperative gastric ultrasonography was performed to assess antral cross-sectional area and gastric volume. Additionally, the study investigated the relationship between gastric ultrasound findings and postoperative complications such as nausea and vomiting. The influence of demographic and clinical variables, including age, body mass index, ASA score, and fetal characteristics, on gastric volume was also evaluated.
Trial Details
NCT Number NCT07513675
Lead Sponsor Dr. Lutfi Kirdar Kartal Training and Research Hospital
Conditions Pregnancy, Ceserean Section, Gastric Volume, Postoperative Nausea and Vomit
Enrollment 90 participants
Start Date 2024-06-01
Primary Completion 2025-06-01 (estimated)
Study Completion 2025-06-01 (estimated)
Updated on ClinicalTrials.gov 2026-04-07