Gastric POCUS for Airway Management in Patients Using Glucagon-like Peptide-1 Receptor Agonist (Multicentric)
Condition(s) studied
Investigational drug(s) / intervention(s)
Gastric Ultrasound: Gastric Ultrasound
Study summary
1\. Introduction
Scheduled surgery requires patients to undergo a preoperative fasting period of at least 6 hours to reduce the risk of perioperative pulmonary aspiration. However, certain medications and conditions may delay gastric emptying, potentially increasing aspiration risk. These include diabetic gastroparesis and the use of glucagon-like peptide-1 (GLP-1) receptor agonists for the treatment of diabetes and obesity.
GLP-1 receptor agonists are widely used due to their beneficial effects on glycemic control and weight reduction. However, one of their known effects is delayed gastric emptying, which may result in increased residual gastric content despite adherence to standard fasting guidelines. Recent reports have described cases of pulmonary aspiration during anesthesia in patients receiving GLP-1 receptor agonists, even after appropriate fasting.
Given the increasing use of these medications, there is a need for objective assessment tools to evaluate gastric content in the perioperative setting. Gastric ultrasonography has emerged as a non-invasive bedside technique that may help identify patients at increased risk of aspiration and guide airway management strategies.
Eligibility
Primary outcome measure(s)
- Gastric Ultrasound — Immediately prior to induction of anesthesia
Gastric ultrasonography performed by trained anesthesiologists, for measuring gastric content in volume (cm3) is a useful tool for assessing gastric content and making clinical decisions regarding airway management.
Trial sites (2)
| Facility | City | Region | Status |
|---|---|---|---|
| Clinica Universidad Navarra | Madrid | Madrid | Recruiting |
| CAUSA Salamanca | Salamanca | Spain | Recruiting |
More Clinica Universidad de Navarra, Universidad de Navarra trials in Spain
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 NCT06666049 on ClinicalTrials.gov ↗ ← All trials in Spain