Current partner codePEPTIDESDE
NCT06533527·Phase 4·INTERVENTIONAL

Holding vs. Continuing Incretin-based Therapies Before Upper Endoscopy

Status

Completed

Phase

Phase 4

Enrollment

69

Locations

2

Results

Posted

Publications

3

Study summary

What the protocol is testing.

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

Treatment arms and agents.

DRUG

GLP-1 medication

Continue taking GLP-1 as normally scheduled prior to endoscopy.

Timeline

From registration to results.

  1. First posted

    Aug 1, 2024

  2. Study start

    Jul 31, 2024

  3. Primary completion

    May 20, 2025

  4. Study completion

    May 20, 2025

  5. Results posted

    Dec 5, 2025

  6. Registry updated

    Dec 5, 2025

Outcomes

What the study measures.

Primary 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

Secondary outcomes

Not reported in the indexed record.

Eligibility

Who can take part.

Minimum age
Not reported
Maximum age
Not reported
Sex
ALL
Healthy volunteers
Yes

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

2 registered sites.

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

Related trials

More studies on Liraglutide.

Related PeptideStat pages

Put the record in context.

Research pages describe evidence. Vendor pages, where available, describe independently tracked research-product listings and are not clinical recommendations.