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The Use of AI to Improve Quality of OGD

Conditions
Dyspepsia
Acid Reflux
Dysphagia
Anemia
Interventions
Diagnostic Test: The use of artificial intelligence system Cerebro
Registration Number
NCT04883567
Lead Sponsor
Chinese University of Hong Kong
Brief Summary

Early and accurate recognition of gastrointestinal lesions has implications for public health. The quality of oesophagogastroduodenoscopy (OGD) has great impact on the detection of oesophageal and gastric malignancies. An AI system, Cerebro, has been developed as a real-time recognition of a pre-defined 28 locations. This system would alert the endoscopist if the sites were not inspected with adequate time. The aim of the study is to investigate the use of AI in endoscopists-in-training during OGD to provide a real-time feedback for ensuring compliance to a standardized protocol for examination. The hypothesis is that the use of AI system Cerebro will significantly improve the compliance to the protocol and thereby reduce the blind spot rates of OGD, ensure adequate inspection time and ensure adequate photodocumentation.

Detailed Description

Not available

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
210
Inclusion Criteria
  1. All patients aged >= 18 years old
  2. Undergoing diagnostic OGD for evaluation of their symptoms in the Prince of Wales Hospital will be included in the study.
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Exclusion Criteria
  1. Patients in which a full endoscopic examination is not required including patients with a specific diagnostic purpose without the need for a full evaluation, follow-up endoscopy within 8 weeks for a previously diagnosed disease or condition,
  2. Patients' condition requiring therapeutic endoscopy,
  3. Early termination of endoscopy due to patient intolerance, presence of large amount of food residue, presence of mechanical obstruction or for reasons of safety,
  4. Patients with altered anatomy such as history of esophagectomy, gastrectomy, gastric bypass surgery, or Whipple's operation,
  5. Patient who are not suitable for EGD examination (such as acute peritonitis with suspected perforated bowel)
  6. Pregnant females
  7. Patients who refuse to participate in the study
  8. Patients who are unfit for consent.
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Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
AI armThe use of artificial intelligence system CerebroAI would be used to assist the trainee endoscopist
Primary Outcome Measures
NameTimeMethod
The number of sites inspected during OGDDuring the procedure

There is a standardised 28 sites the trainee endoscopist need to inspect

Secondary Outcome Measures
NameTimeMethod
The number of positive pathologies found on OGDduring the procedure

The number of positive pathologies found on OGD would be recorded

The individual sites inspection timeDuring the procedure

The individual inspection time of the 28 sites during OGD would be recorded in terms of seconds

Overall inspection timeDuring the procedure

The overall inspection time during the OGD would be recorded in terms of seconds

Trial Locations

Locations (1)

The Chinese University of Hong Kong

🇭🇰

Hong Kong, Hong Kong

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