Preoperative Fasting Duration and Gastric Residue in Pediatric Upper Gastrointestinal Endoscopy

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age0-17
SponsorBursa Sevket Yilmaz Training and Research Hospital

About this trial

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.

Eligibility criteria

Qualifiers

Pediatric patients aged under 18 years

Patients who underwent upper gastrointestinal endoscopy for gastrointestinal symptoms or pathology

Patients with available hospital records, anesthesia records, and endoscopy reports

Patients with documented preoperative fasting duration

Disqualifiers

Patients aged 18 years or older

Patients with missing or incomplete data for key study variables

Patients without documented preoperative fasting duration

Patients without documented gastric residue assessment during endoscopy

Trial design

Treatments tested in this trial

  • Upper Gastrointestinal Endoscopy

Treatment groups

110 Participants
are divided into 1 treatment group