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Accuracy of Gastric Ultrasound to Diagnose a Full Stomach. A Bayesian Framework

Accuracy of Gastric Ultrasound to Diagnose a Full Stomach. A Bayesian Framework

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02588495
Enrollment
80
Registered
2015-10-27
Start date
2015-10-26
Completion date
2017-06-30
Last updated
2017-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Aspiration

Keywords

Ultrasound, Gastric area, Accuracy, Aspirate

Brief summary

During surgery, there is a risk that food or liquid in the stomach might be forced back up the throat where it could enter the lungs (aspirate) and result in serious complications or even death. This is why people going for surgery are required not to eat before their surgery. However, in emergency situations it is often not possible to know whether a patient has recently eaten or not. Anesthesiologists have recently developed an ultrasound test to determine if there is content in a patient's stomach and how much. This test involves an ultrasound examination of the abdomen and taking some measurements on the ultrasound screen. The purpose of this study is to determine how accurate these measurements are. In other words, how good are we at detecting an empty stomach from one that has liquids, or solids in it. You are being asked to participate in this study because we require non-pregnant volunteers in order to answer the aforementioned study question.

Interventions

OTHERFood intake

Either drinking a cup of clear liquid, or having a cup of coffee and a muffin

Sponsors

University Health Network, Toronto
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
Yes

Inclusion criteria

* Healthy volunteers aged 18 to 85 years * Male or female * American Society of Anesthesia physical status classification I and II * Height greater than 145 cm * Ability to understand the study protocol and provide informed consent

Exclusion criteria

* Subjects predisposed to have an increased residual gastric volume at baseline (eg. Diabetes or any known dysmotility) * History of major upper gastrointestinal disease (including hiatus hernia or prior gastroduodenal surgery)

Design outcomes

Primary

MeasureTime frameDescription
Ultrasound's sensitivity to identify a full stomach5 minutesScanning the stomach to identify if the participant is fasted or has ingested liquid or solids

Secondary

MeasureTime frameDescription
Ultrasound's accuracy in detecting a full stomach5 minutesAssessing how accurate the Ultrasound machine is in detecting either liquid or solid contents in the participant's stomach after ingestion
Inter/Intra-rater reliability of observer in detecting a full stomach5 minutesDetermining the reliability of observers in being able to similarly detect a full stomach

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026