CompletedNot Applicable

GLP-1 Receptor Agonist Use and Incidence of Retained Gastric Food on Endoscopy

United States260 participantsStarted 2023-08-21

Plain-language summary

This study will enroll patients ages 18 and over who are in one of the following groups 1) taking a GLP-1 receptor agonist medication 2) not taking a GLP-1 receptor agonist (control group), are undergoing EGS and have appropriately fasted. Study data will be collected in the form of qualitatively observing whether the stomach is empty as expected, or contains solid or clinically relevant liquid contents.

Who can participate

Age range18 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria * Adults 18 years of age and older presenting for esophagogastroduodenoscopy (EGD) * One of the following groups: * GLP-1 receptor agonist cohort: active treatment with any GLP-1 receptor agonist therapy within prior 30 days * Control cohort: not taking a GLP-1 receptor agonist medication * Appropriately fasted per ASA Fasting Guidelines Exclusion Criteria * Simultaneous bowel preparation/planned dual endoscopy with colonoscopy * Any pre-planned alteration to standard fasting guidelines (ASA NPO guidelines) * Emergency endoscopic procedure * Concern for active GI bleeding * Food impaction/foreign body as indication for procedure * Gastric outlet obstruction/bowel obstruction * Achalasia * Zenker's diverticulum * History of esophageal or gastric surgery * Active pregnancy * Chronic daily opioid therapy ≥ 15 MMEs per day * Prokinetic agent use (i.e. metoclopramide) * Inability or unwillingness of subject to give informed consent

What they're measuring

Retained gastric food

Timeframe: From time of enrollment until the end of surgery, assessed up to 4 weeks

Trial details

NCT IDNCT05875636

SponsorMedical University of South Carolina

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2024-08-23