DRUG
GLP-1 medication
Continue taking GLP-1 as normally scheduled prior to endoscopy.
Status
Completed
Phase
Phase 4
Enrollment
69
Locations
2
Results
Posted
Publications
3
Study summary
To assess whether holding incretin-based therapy before endoscopy reduces the likelihood of clinically relevant Residual Gastric Volume (RGV). Primary Outcomes: * Residual gastric volume that precludes adequate endoscopic examination * Residual gastric volume that necessitates premature termination of the endoscopy procedure * Need for endotracheal intubation due to stomach contents. * Occurrence of aspiration events requiring extended observation/monitoring, unplanned therapeutics, and/or hospital admission Secondary Outcomes: * Presence of any solid food * Presence of moderate liquid content * Increased RGV(Residual Gastric Volume) defined as any amount of solid content or \> 0.8 mL/Kg of fluid content (measured from the aspiration/suction canister). * Differences in primary and secondary outcomes between different medications
Interventions
DRUG
Continue taking GLP-1 as normally scheduled prior to endoscopy.
Timeline
First posted
Aug 1, 2024
Study start
Jul 31, 2024
Primary completion
May 20, 2025
Study completion
May 20, 2025
Results posted
Dec 5, 2025
Registry updated
Dec 5, 2025
Outcomes
Presence of RGV (Residual Gastric Volume) in Stomach
Time frame · Procedure
Residual gastric volume (RGV) that precludes adequate endoscopic examination
Tracking the Use of Intubation Due to RGV
Time frame · Procedure
Aspiration Events Due to RGV (Residual Gastric Volume)
Time frame · Procedure
Occurrence of aspiration events requiring extended observation/monitoring, unplanned therapeutics, and/or hospital admission
Not reported in the indexed record.
Eligibility
Inclusion Criteria: * Patients using incretin-based therapies at a stable dose for more than 1 month. * Patients scheduled for outpatient esophagogastroduodenoscopy (EGD), endoscopic ultrasound (EUS), or endoscopic retrograde cholangiopancreatography (ERCP) under monitored anesthesia care. Exclusion Criteria: * Documented history of gastroparesis (based on a 4-hour solid-phase gastric emptying study) * Known history of achalasia * Surgical or genetically altered foregut anatomy * Known gastric outlet obstruction or pre-procedure imaging suggestive of gastric outlet obstruction. * Patients who did not follow the standard NPO (nil per oral) instructions.
Study locations
United States. Showing up to 24 locations stored in the fast local snapshot.
Cleveland Clinic
Weston, Florida, United States
Cleveland Clinic
Cleveland, Ohio, United States
Publications
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Related PeptideStat pages
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