Gastric Content in Fasting Volunteers and in Tirzepatide Users: an Observational and Cross-sectional Study

Recruiting now

Conditions studied: Full Stomach Status

In brief

Introduction Obesity and type 2 diabetes mellitus constitute a global public health problem. Medications with glucagon-like peptide-1 (GLP-1) receptor agonist activity are a modern therapeutic option for both diseases. Liraglutide, semaglutide, dulaglutide and tirzepatide are representatives of this drug class, whose mechanism of action results in delayed gastric emptying, reduced gastric motility and increased gastric volume. Tirzepatide, however, presents a dual agonist action, combining GLP-1 agonism with glucose-dependent insulinotropic polypeptide (GIP) agonism. The presence of gastric content during anaesthesia may lead to pulmonary aspiration and the development of chemical pneumonitis, a potentially devastating complication. However, when there is a risk factor for delayed gastric emptying, despite adequate fasting, the stomach may still present residual content, and bedside ultrasonography is an effective, non-invasive and rapid method to measure this content and stratify aspiration risk. Our hypothesis is that most individuals using tirzepatide present a full stomach even after fasting times recommended in the literature.

Key facts

Study ID
NCT07398222
Run by
Hospital Israelita Albert Einstein
People needed
30
Starts
2026-01-26
Expected to finish
2026-03-20
Last updated by the study team
2026-02-09

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: accepted.

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Where it is running

Full record on ClinicalTrials.gov

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