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RecruitingNCT06814080

Residual Gastric Content and GLP-1

Status
Recruiting
Phase
Study type
Observational
Enrollment
45 (estimated)
Sponsor
University of Arkansas · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

Studies have shown that even following the fasting guideline, patients on GLP-1 still have residual gastric content which increases their risk of aspiration during anesthesia. We aim to investigate the prevalence of full stomachs following different fasting times.

Detailed description

Glucagon-like peptide-1 (GLP-1) receptor agonists have become increasingly popular as both diabetic and weight loss therapies. One effect of this class of medication is delayed gastric emptying, which may impact the risk of aspiration during anesthesia delivery. Some of them have a very long half-life of approximately one week. Thus, it takes approximately five weeks to achieve its steady-state concentration, and just as long for its effects to terminate after stopping the drug. As a standard of care, patients are allowed to drink up to 2 hours and to eat up to 8 hours before surgery. Studies have shown that even following the fasting guideline, patients still have residual gastric content which increases their risk of aspiration during anesthesia. Since stopping these drugs for a long time is not practical as it is going to disrupt their glycemic control and reverse the weight loss, we propose to test extending the fasting time. We aim to investigate the prevalence of full stomachs following different fasting times. patients will be assigned to one of three groups: Group 1(G1) with 8-hour fasting, Group 2 (G2) with 10-hour fasting, and Group 3 (G3) groups with 12-hour fasting

Conditions

Timeline

Start date
2025-05-22
Primary completion
2026-08-01
Completion
2026-08-01
First posted
2025-02-07
Last updated
2025-09-18

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT06814080. Inclusion in this directory is not an endorsement.