RecruitingPhase NA

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

Lead sponsor

Mayo Clinic

Asset

GLP-1 / incretin class catch-all

Listed sites

Recruiting sites

Estimated enrollment

150

Study population

Eligibility highlights

Primary endpoint

•Gastric contents

Registered trial locations

Locations reported to ClinicalTrials.gov for this trial snapshot. Site count is not enrollment count; per-site enrollment is not available from source.

Identifiers

Registered as

NCT IDNCT07006142

Org study ID23-013192

Timeline

Milestones

Study first posted2025-06-05actual

Study start2025-08-01actual

Last update posted2026-06-03actual

Primary completion2026-08-30estimated

Study completion2026-08-30estimated

Assets

Investigational agents

GLP-1 / incretin class catch-all

Who can enroll

Minimum age18 Years

SexAll

Healthy volunteersNot accepted

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

Endpoints (4)

What's being measured

Protocol endpoints and posted registry outcome measures, grouped into outcome categories. Composite endpoints show their component event types. Standard codes (LOINC, SNOMED CT) are shown where available.

Other (unclassified)

4 endpoints

Primary/protocol endpoint/low confidence

Gastric contents

Time frame:Baseline

descriptive

Secondary/protocol endpoint/low confidence

Diagnosis of aspiration within 72 hours of procedure

Time frame:From the time of upper endoscopy until 72 hours post-procedure.

ratio, improvement

Secondary/protocol endpoint/low confidence

Aspiration pneumonitis diagnosis postoperatively

Time frame:72 hours after completion of upper endoscopy

ratio, improvement

Secondary/protocol endpoint/low confidence

Postprocedural ICU admission

Time frame:Immediately after upper endoscopy

descriptive

Provenance

Sources

Trial identity, design, statusClinicalTrials.gov API v2

Snapshot dateJuly 6, 2026

Endpoint classificationDelfa endpoint taxonomy v2 (May 13, 2026)

Results tableno registry results posted yet

Trial facts come from public ClinicalTrials.gov records. Endpoint categories are Delfa's classification of those records, not a ClinicalTrials.gov field. All figures reflect the July 6, 2026 snapshot.