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Clinical Trials in Turkey / NCT07483593
Starting soon Observational

Baseline Gastric Volume in Diabetic vs Non-Diabetic Patients

NCT07483593 · tracked via the Priya Life Science Turkey tracker
Phase
Observational
Started
2026-04-20
Last updated
2026-03-19

Condition(s) studied

Gastric VolumePreoperative FastingDiabetes Mellitus

Investigational drug(s) / intervention(s)

Gastric Ultrasound

Gastric Ultrasound: Preoperative gastric ultrasonography will be performed to assess gastric antral cross-sectional area and estimate residual gastric volume in patients scheduled for elective surgery. The examination will be performed in the supine and right lateral decubitus positions using a low-frequency convex probe by experienced anesthesiologists.

Study summary

During the preoperative preparation process, the fasting period for anesthesia is planned according to guidelines. According to standard guidelines, a fasting period of at least 2 hours is recommended for clear liquids, at least 6 hours for light meals, and at least 8 hours for a full meal. However, it has been reported that these guidelines are valid for healthy patients. It is thought that the planned fasting periods may vary in diabetic patients due to delayed gastric emptying. This study aims to calculate gastric volume under ultrasonography guidance and compare it with fasting time.

Eligibility

Sex
ALL
Min age
18 Years
Max age
75 Years
Healthy volunteers
No
Inclusion Criteria: * Ages 18-75 * ASA I-III * BMI ≤ 40 kg/m2 Exclusion Criteria: * Patients with a history of gastrointestinal surgery, * Pregnant women, * Patients with documented abnormalities in the upper gastrointestinal tract, such as achalasia

Primary outcome measure(s)

Trial sites (2)

FacilityCityRegionStatus
Kocaeli University Kocaeli Turkey (Türkiye)
Sevim Cesur Kocaeli Turkey (Türkiye)

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Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07483593 on ClinicalTrials.gov ↗ ← All trials in Turkey