Gastric Emptying With Metoclopramide in GLP-1 Agonist Patients Undergoing Elective Surgery

Trial statusNot yet recruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexAll
Age18+
SponsorMater Misericordiae University Hospital

About this trial

This is a multicentre, investigator-blinded, randomised controlled trial evaluating whether the use of oral metoclopramide before surgery can reduce the amount of residual gastric content in patients who are taking glucagon-like peptide-1 receptor agonists (GLP-1 RAs) for weight loss. These medications are known to slow down gastric emptying, which may increase the risk of pulmonary aspiration during anaesthesia. Patients will be randomly assigned to either receive metoclopramide 24 hours before surgery or continue with standard care. The primary outcome will be the presence or absence of residual gastric content on ultrasound before surgery. Secondary outcomes include nausea, vomiting, constipation, and any adverse effects of the medication.

Eligibility criteria

Qualifiers

Patients taking GLP-1 receptor agonists (for weight loss only)

Male and female patients aged 18 years or older

Able to provide written informed consent

ASA grade I-V

Disqualifiers

Inability to provide informed consent

Presence of hiatus hernia

History of any gastric surgery

Pregnancy

Trial design

Treatments tested in this trial

  • Metoclopramide

Treatment groups

80 Participants
are divided into 2 treatment groups