Condition: Residual Gastric Contents · Pulmonary Aspiration of Gastric Contents · Sponsor: St Vincent's Hospital Melbourne
The aim of this randomised controlled trial is to determine the effect of a 24-hour clear liquid diet compared to standard fasting guidelines on the proportion of participants who present with increased residual gastric contents during their study visit. It also aims to determine the effect of a 24-hour clear liquid diet compared to standard fasting guidelines on: * Solid content or thick fluids * Patient-reported outcome measures (PROMs), including thirst, hunger, nausea, fatigue, and anxiety. * Compliance measures, including adherence with the intervention, time since last oral intake of solid foods, and time since last oral intake of clear liquids. We will enrol adults who are currently using any once-weekly glucagon-like peptide-1 receptor agonist (GLP-1RA) medication. Participants will be allocated in a 1:1 ratio to follow a 24-hour clear liquid diet or standard fasting guidelines prior to attending a study visit where participants will undergo a blinded gastric ultrasound assessment.
This description comes directly from the study's public registry record.
Prof Michelle Dowsey, BHealthSci(Nursing), MEpi, PhD · 03 9231 3955 · mmdowsey@unimelb.edu.au
Jasmin Elkin · jelkin@student.unimelb.edu.au
Always discuss trial participation with your own doctor first.
| Melbourne Gastro Oesophageal Surgery (MGOS) | Melbourne, Victoria, Australia | Recruiting |
| St Vincent's Hospital Melbourne | Melbourne, Victoria, Australia | Recruiting |
Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.
We email about this public record only. Unsubscribe anytime with one click. Never medical advice.
This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.
Source record: clinicaltrials.gov/study/NCT06839248