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A Deep Learning Approach to Identify Patients With Full Stomach on Ultrasonography

Not Applicable
Recruiting
Conditions
Gastic Antrum
Interventions
Dietary Supplement: Intervention oral supplement
Registration Number
NCT05846607
Lead Sponsor
Huashan Hospital
Brief Summary

Preoperative gastric ultrasonography is a newly developed tool used to evaluate gastric content and volume in assessing perioperative aspiration risk and guide anaesthetic management. And then build up effective clinical predictive models for identification of full stomach, which can predict the high aspiration risk.

Detailed Description

Aspiration of gastric contents can be a serious anesthetic related complication. Preoperative fasting was a common practice to decrease perioperative aspiration risk. However,one of most important prescription of enhanced recovery after surgery protocols is the reduction of preoperative fasting time in opposition to the traditional recommendation of overnight fast. Gastric antral sonography prior to anesthesia may have a role in identifying patients at risk of aspiration. The aim of this study is to construct models using deep learning for identification of full stomach, which can predict the aspiration risk.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
800
Inclusion Criteria

Patients undergoing surgery Age: 18~85 yeas ASA 1~3

Exclusion Criteria

-Diabetes mellitus Upper gastrointestinal pathology such as hiatus hernia, oesophageal cancer Prior surgery to upper GI On medication that may affect gastric emptying time Pregnancy

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
experimentIntervention oral supplementThe data will be collected in two phases. Firstly, after a fasting period of eight hours, the participants received ultrasound scan by expert doctor with the objective of measuring the fasting gastric antrum area in supine and right lateral decubitus(RLD)position(phase 1).Then the expert made the grading according to the ultrasound image. In phase 2, the participant will ingest 0 to 400ml of the study drink described below randomly. The individual will be immediately positioned in the supine position and another ultrasound scan will be carried out. Again in the RLD position.
Primary Outcome Measures
NameTimeMethod
Diagnostic accuracy of the model1 year
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Fudan University affiliated Huashan Hospital

🇨🇳

Shanghai, China

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