Residual Gastric Content After Holding of Glucagon-like Peptide-1 Receptor Agonists Before Elective Surgery
NCT ID: NCT06500143
Last Updated: 2026-01-16
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
94 participants
OBSERVATIONAL
2024-10-09
2025-02-28
Brief Summary
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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
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Detailed Description
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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
Secondary objectives:
* To assess the relation between the number of days since the last dose of GLP-1RA and increased RGC
* To assess the relation between the dose of GLP-1RA and RGC
Exploratory objectives:
* To explore the relation between other known risk factors of gastroparesis and increased RGC
* To explore the relation between the time since the last oral intake and increased RGC
Methods : A gastric ultrasound (GUS)will be performed on all patients to assess RGC using a published validated and reproductible method used in recent trials. The acquisition of images will be performed by a blinded anesthesiologist or anesthesiology resident using a dedicated ultrasound machine. The images will be saved and reviewed by another blinded trained anesthesiologist.
Significance/importance: The results of this study could challenge the actual recommendations for GLP-1RA stoppage before surgery and help improve perioperative care for patients taking GLP-1RA.
Conditions
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Study Design
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OTHER
CROSS_SECTIONAL
Study Groups
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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
Gastric ultrasound
Using a curved array low-frequency abdominal probe (2-5 MHz) with abdominal presets and with the patient in right lateral decubitus position, the gastric antrum will be identified in a standardized plane at the level of the aorta. The stomach will be considered empty if the antrum appears flat or round with anterior and posterior walls collapsed. Normal gastric secretions and clear fluids have an anechoic or hypoechoic aspect on ultrasonography. Solid or thick fluids have a hyperechoic aspect and can create "ring-down" artifacts blurring gastric content, its posterior wall, the pancreas and the aorta. Following qualitative examination, quantitative assessment will be performed if there is presence of clear fluids. The cross-sectional area (CSA) of the antrum will be measured with three measurements to calculate a mean value.
Control group
Participants presenting for elective surgery and not taking semaglutide or dulaglutide
Gastric ultrasound
Using a curved array low-frequency abdominal probe (2-5 MHz) with abdominal presets and with the patient in right lateral decubitus position, the gastric antrum will be identified in a standardized plane at the level of the aorta. The stomach will be considered empty if the antrum appears flat or round with anterior and posterior walls collapsed. Normal gastric secretions and clear fluids have an anechoic or hypoechoic aspect on ultrasonography. Solid or thick fluids have a hyperechoic aspect and can create "ring-down" artifacts blurring gastric content, its posterior wall, the pancreas and the aorta. Following qualitative examination, quantitative assessment will be performed if there is presence of clear fluids. The cross-sectional area (CSA) of the antrum will be measured with three measurements to calculate a mean value.
Interventions
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Gastric ultrasound
Using a curved array low-frequency abdominal probe (2-5 MHz) with abdominal presets and with the patient in right lateral decubitus position, the gastric antrum will be identified in a standardized plane at the level of the aorta. The stomach will be considered empty if the antrum appears flat or round with anterior and posterior walls collapsed. Normal gastric secretions and clear fluids have an anechoic or hypoechoic aspect on ultrasonography. Solid or thick fluids have a hyperechoic aspect and can create "ring-down" artifacts blurring gastric content, its posterior wall, the pancreas and the aorta. Following qualitative examination, quantitative assessment will be performed if there is presence of clear fluids. The cross-sectional area (CSA) of the antrum will be measured with three measurements to calculate a mean value.
Eligibility Criteria
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Inclusion Criteria
* 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
* Inability to lay on the right-side for ultrasound
* Pregnancy
* History of gastric surgery or large hiatal hernia
18 Years
ALL
Yes
Sponsors
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Institut de Cardiologie de Montréal
UNKNOWN
Ciusss de L'Est de l'Île de Montréal
OTHER
Responsible Party
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Principal Investigators
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Louis Morisson, MD, MSc
Role: PRINCIPAL_INVESTIGATOR
CIUSS de l'Est de l'Île de Montréal
Locations
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CIUSSS de l'Est de l'Ile de Montréal
Montreal, Quebec, Canada
Countries
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Other Identifiers
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MP-12-2025-3794
Identifier Type: -
Identifier Source: org_study_id
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