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Preoperative Fasting Duration and Gastric Residue in Pediatric Upper Gastrointestinal Endoscopy

StatusNot Yet Recruiting
PhaseNot specified
Started
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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.

Record History

  1. Study First Submitted
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
(from sponsor)		 Gastric Residue, Preoperative Fasting, Upper Gastrointestinal Endoscopy
Related terms Fasting
Enrollment 110 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov