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Clinical Trials/NCT06500143
NCT06500143CompletedNot Applicable

The RESIDUAL Study : Residual Gastric Content After Holding of Glucagon-like Peptide-1 Receptor Agonists Before Elective Surgery: a Cross-sectional Study

Ciusss de L'Est de l'Île de Montréal1 site in 1 country94 target enrollmentStarted: October 9, 2024Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
94
Locations
1
Primary Endpoint
Increased residual gastric content

Study Overview

Brief Summary

Glucagon-like peptide-1 agonists (GLP-1RA) are a family of medications used for diabetes and weight loss. One of their effect is to slow down stomach emptying. The goal of this study is to evaluate the effect of GLP-1RA on the effectiveness of fasting before a scheduled surgery.

The question it aims to answer is: does this kind of medication increase the risk of having food or too much liquid in the stomach before a scheduled surgery, even if the minimum 6 hour fast is done?

For this project, researchers will use gastric ultrasound to compare participants already taking one of these medications as part of their home treatment to participants who are not taking them. Gastric ultrasound is a simple bedside exam using an echography machine that takes less than 5 minutes to do.

Participants will:

-Have a gastric ultrasound performed on them before their surgery

Detailed Description

Background: Glucagon-like peptide-1 receptor agonists (GLP-1RA) are glucose-lowering drugs that act through three mechanisms: stimulation of insulin secretion, inhibition of glucagon secretion and decrease of gastric emptying. The GLP-1RA are now an important part of glycemic control in type 2 diabetes mellitus (T2DM). Recently, GLP-1 RA have received approval for weight loss, expanding their use in overweight or obese non-diabetic patients.The effect of GLP-1RA on decreased gastric emptying has long been established but he clinical implication of this in the periprocedural setting is uncertain. Recent guidelines recommend holding the weekly-dosed for at least a week before elective surgery. Considering the extended half-lives of once-weekly GLP-1RA (approximately 6 days for semaglutide and 5 days for dulaglutide), it is unclear if following those guidelines is sufficient to make sure patients are not at high risk of aspiration

Hypothesis: This study will compare ultrasound-assessed residual gastric content (RGC) between once-weekly GLP-1RA users that stopped their medication for 7 days or more before elective surgery and patients not taking GLP-1RA. The investigators hypothesized that even with appropriate holding of GLP-1RA, those patients may have increased RGC and be at higher risk of aspiration.

Objectives:

Primary objective:

• To investigate the relation between GLP-1RA use and increased RGC

Study Design

Study Type
Observational
Observational Model
Other
Time Perspective
Cross Sectional

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • American Society of Anesthesiologists (ASA) class 1-4 patients
  • Age ≥ 18 years old
  • Fasted state (2 hours for clear liquids, 6 hours for solids)
  • Elective surgery
  • Last dose of once-weekly semaglutide or dulaglutide 7 days or more before surgery (for GLP-1RA group)

Exclusion Criteria

  • Last dose of GLP-1RA less than 7 days before surgery
  • Inability to lay on the right-side for ultrasound
  • Pregnancy
  • History of gastric surgery or large hiatal hernia

Arms & Interventions

GLP-1RA agonists users

Participants presenting for elective surgery and taking once-weekly semaglutide or dulaglutide as part of their usual treatment with the last dose at least 7 days before surgery

Intervention: Gastric ultrasound (Diagnostic Test)

Control group

Participants presenting for elective surgery and not taking semaglutide or dulaglutide

Intervention: Gastric ultrasound (Diagnostic Test)

Outcomes

Primary Outcomes

Increased residual gastric content

Time Frame: Preoperative (day of surgery)

The primary endpoint will be the prevalence of increased residual gastric content defined by the presence of any of the following: * Solid or thick fluid content on gastric ultrasound * Content of more than 1.5 mL/kg of clear fluids on gastric ultrasound using the following formula : Gastric volume (mL) = 27 + \[14.6 × right lateral cross-sectional area (in cm2)\] - \[1.28 × age (in years)\]

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Ciusss de L'Est de l'Île de Montréal
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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