Fasting Time Effects for Patients on GLP1 Receptor Agonists

Effect of Prolonged Fasting Time on Gastric Residual Volume in Patients Taking GLP1 Receptor Agonists

Recruiting N/A Interventional Study
Upper Endoscopy GLP1-R-related Disease
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Prevention
Participants needed
150 (estimated)
Sponsor
Mayo Clinic · Other
Who this trial is looking for

This trial is looking for patients who are scheduled for an upper endoscopy. Participants will help researchers understand if changing fasting times can lower the risk of aspiration during the procedure.

Are You a Good Fit for This Trial?

You may be able to join if

  • I am scheduled for an elective upper endoscopy.

You may not be able to join if

  • I need an urgent or emergency procedure.
  • My procedure includes a colonoscopy or small bowel enteroscopy.
  • I had an upper GI barium study in the past 24 hours.
  • I have gastroparesis.
  • I have achalasia.
  • I have pancreatitis.
  • I take pro-motility medications.
  • I cannot provide my own consent.

Summarized in plain language from this trial's official eligibility criteria. The full criteria are further down this page — only the research team can confirm whether you qualify.

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About This Trial

The aim of this study is to determine whether a modified fasting protocol can reduce the potential risk of aspiration for patients currently prescribed GLP1-RAs.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Patients undergoing elective upper endoscopy with gastroenterology team Exclusion Criteria: * Urgent or emergent procedure * Inclusion of colonoscopy or antegrade small bowel enteroscopy in planned procedure * Upper GI barium study performed in past 24 hours. * Gastroparesis…
Contacts

Krishnan Ramanujan, MD

507-422-4898

ramanujan.krishnan@mayo.edu

CONTACT