Suspended

Usefulness of Artificial Intelligence (AI) for Gastric Intestinal Metaplasia Diagnosis

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What is being tested

Artificial intelligence

Diagnostic Test
Who is being recruted

Over 18 Years
+5 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Diagnostic Study

Interventional
Study Start: May 2020
See protocol details

Summary

Principal SponsorKing Chulalongkorn Memorial Hospital
Study ContactRapat Pittayanon, MD
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: May 1, 2020

Actual date on which the first participant was enrolled.

The patients with previously diagnose gastric intestinal metaplasia (GIM) and have the surveillance gastroscopy will be enrolled. The routine surveillance program will be performed additional to taking photo at both GIM and normal mucosa at least 5 pictures in each. Biopsy will be done to confirm the diagnosis of GIM and normal mucosa. All pictures will be inserted to AI algorithm based on the convolutional neural network (CNN). Then, the AI program will be validated in daily endoscopy compared with pathology. Accuracy, sensitivity and specificity can be calculated by 2x2 table.

Official TitleUsefulness of Artificial Intelligence (AI) for Gastric Intestinal Metaplasia Diagnosis
Principal SponsorKing Chulalongkorn Memorial Hospital
Study ContactRapat Pittayanon, MD
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

120 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Diagnostic Study

Diagnostic studies focus on improving how we detect or confirm a disease. They test new tools or techniques that could provide faster or more accurate diagnoses.



Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

Over 18 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Criteria

2 inclusion criteria required to participate
More than 18 years of age

Able to sign a consent form

3 exclusion criteria prevent from participating
History of gastric surgery

Coagulopathy

Pregnancy/Breast feeding

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

One single intervention group is designated in this study

This study does not include a placebo group 

Treatment Groups

Group I

Experimental
The patients with GIM will be assessed at both GIM and normal mucosa during endoscopy.

Study Objectives

Primary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Recruiting

Rapat Pittayanon

Pathum Wan, ThailandOpen Rapat Pittayanon in Google Maps
SuspendedOne Study Center
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