Clinical Trial

Preoperative Fasting Duration and Gastric Residue in Pediatric Upper Gastrointestinal Endoscopy

Not Yet Recruiting

Record status

This record was last updated May 29, 2026 (before its estimated July 1, 2026 completion). Its status may not reflect the trial's current state.

Summary

This retrospective observational study aims to evaluate the relationship between preoperative fasting duration and gastric residue in pediatric patients undergoing upper gastrointestinal endoscopy for gastrointestinal symptoms or pathology. The study will assess the associations between gastric residue, gastrointestinal symptoms, underlying gastrointestinal diseases, and endoscopic findings. Data will be retrospectively collected from hospital records, anesthesia records, and endoscopy reports to investigate whether prolonged fasting duration reliably predicts an empty stomach in pediatric gastrointestinal patients.

Trial Details

NCT Number	NCT07614919
Lead Sponsor	Bursa Sevket Yilmaz Training and Research Hospital
Conditions	Gastric Residue, Preoperative Fasting, Upper Gastrointestinal Endoscopy
Enrollment	110 participants
Start Date	2026-06-01
Primary Completion	2026-07-01 (estimated)
Study Completion	2026-07-01 (estimated)
Updated on ClinicalTrials.gov	2026-05-29