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

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Mayo Clinic

Status

Enrolling

Conditions

GLP1-R-related Disease
Upper Endoscopy

Treatments

Other: Modified Fasting Guidelines

Study type

Interventional

Funder types

Other

Identifiers

NCT07006142
23-013192

Details and patient eligibility

About

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.

Full description

The overall objective of this project is to identify a reasonable means by which patients on GLP1-RAs can be safely cared for in the perioperative period that can be agreed upon by all groups involved in perioperative patient care. This will be assessed in patients undergoing upper endoscopy specifically since assessment of gastric contents would be minimally invasive for this patient population receiving anesthetic care.

Enrollment

150 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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
  • Achalasia
  • Pancreatitis
  • Use of outpatient pro-motility medications
  • Patient refusal
  • Inability for patient to provide own consent

Trial design

Primary purpose

Prevention

Allocation

N/A

Interventional model

Single Group Assignment

Masking

Single Blind

150 participants in 3 patient groups

Normal fasting guidelines and not taking GLP1-RAs
No Intervention group
Description:
Patients who are not taking GLP1 RAs (Receptor Agonists) and who will abide by the normal fasting guidelines
Normal fasting guidelines with GLP1-RAs
No Intervention group
Description:
Patients who are taking GLP1 RAs (Receptor Agonists) for either diabetes or weight loss management who will abide by normal fasting guidelines
Modified fasting guidelines with GLP1-RAs
Experimental group
Description:
Patients who are prescribed and taking GLP1 RAs (Receptor Agonists) for either diabetes or weight loss management who follow the modified fasting guidelines. Modified fasting consists of a full-liquid diet 48 hours prior to the procedures, clear liquid diet 24 hours prior to their procedure, and nothing by mouth (NPO) after midnight on the day of their procedure.
Treatment:
Other: Modified Fasting Guidelines

Trial contacts and locations

1

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Central trial contact

Krishnan Ramanujan, MD

Data sourced from clinicaltrials.gov

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