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RecruitingNCT07257796Updated Dec 2, 2025

Artificial Intelligence in Assessing Gastric Intestinal Metaplasia Via the EGGIM Score

An observational study in Intestinal Metaplasia of Gastric Mucosa, Artificial Intelligence and Endoscopy, sponsored by Qilu Hospital of Shandong University. Recruiting at 3 sites in China. Open to participants aged 40 Years to 75 Years. Per ClinicalTrials.gov, last updated 2025-12-02.

Sponsored by Qilu Hospital of Shandong University · Observational

From the registry’s dates

  • Started Nov 2025; still recruiting 11 months later.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
3,000
Ages
40 Years to 75 Years
Sex
All
01

Study summary

The endoscopic grading system (EGGIM) has been widely used to assess the extent of gastric intestinal metaplasia during endoscopy. Investigators developed an artificial intelligence (AI) system to automatically evaluate the extent of gastric intestinal metaplasia (GIM) and calculate the EGGIM scores in endoscopy examination. This study is a prospective, multi-center study aimed at exploring the performance and reliability of AI-EGGIM scoring.

This is a prospective study designed to validate the AI-EGGIM system in a larger cohort. The study protocol was developed based on preliminary experience from a prior investigation (NCT05464108).

Read the detailed description

Gastric intestinal metaplasia (GIM) is an important precancerous stage in the gastric carcinogenesis cascade. The endoscopic grading system (EGGIM) has been proposed as a practical method to evaluate the extent of GIM during endoscopy. Investigators developed an artificial intelligence (AI) system to automatically assess the extent of GIM and calculate EGGIM scores from endoscopic examinations. This study is a prospective, multi-center study aimed at evaluating the accuracy, performance, and reliability of AI-assisted EGGIM scoring.

02

Conditions studied

  • Intestinal Metaplasia of Gastric Mucosa
  • Artificial Intelligence
  • Endoscopy
03

In context

Lead sponsor

Qilu Hospital of Shandong University is the lead sponsor of 299 studies on the registry; 181 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
40 Years to 75 Years
Sexes eligible
All
Sampling method
Non-probability sample

Study population

Consecutive patients who receive the gastrointestinal endoscopy examination and screened that fulfill the eligibility criteria will be enrolled into the study.

Inclusion criteria

  • patients aged 40-75 years who undergo the IEE examination
  • patients who voluntarily sign the informed consent form

Exclusion criteria

Exclusion Criteria:

  • patients with severe cardiac, cerebral, pulmonary or renal dysfunction or psychiatric disorders who cannot participate in gastroscopy
  • patients with previous surgical procedures on the stomach
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
3,000 participants (estimated)
Patient registry
No

Interventions

  • Diagnostic testThe diagnostic performance of AI system and endoscopists

    Eligible patients will undergo independent EGGIM score assessment by both endoscopists and the AI system.

06

What researchers measure

Primary outcomes

  1. Performance of AI system to diagnose the grade of intestinal metaplasia by calculating the EGGIM score

    The performance of the AI system will be evaluated in diagnosing the grade of gastric intestinal metaplasia (IM) based on the Endoscopic Grading of Gastric Intestinal Metaplasia (EGGIM) system. EGGIM is a validated scoring method ranging from 0 to 10, reflecting the extent of IM across five gastric regions: two in the antrum, two in the corpus, and one at the incisura. Each region is scored as 0 (no IM), 1 (focal IM, ≤30% of the area), or 2 (extensive IM, \>30% of the area), with a total possible score of 10. Higher EGGIM scores correspond to more severe IM and greater gastric cancer risk. The AI-derived scores will be compared with expert' EGGIM scores, which serve as the gold standard, to assess diagnostic accuracy.

    Time frame: 1 year

07

Study locations

1 of 3 sites recruiting
  • Qilu Hospital of Shandong University
    Jinan, Shandong 250012, China
    Recruiting
  • Shandong First Medical University First Affiliated Hospital
    Jinan, Shandong, China
    Not yet recruiting
  • Shandong Second Provincial General Hospital
    Jinan, Shandong, China
    Not yet recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 2, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07257796
Lead sponsor
Qilu Hospital of Shandong University
Responsible party
Sponsor
First posted
Dec 2, 2025
Start date
Nov 1, 2025
Primary completion
May 31, 2027 (estimated)
Completion
Dec 31, 2027 (estimated)
Last update
Dec 2, 2025

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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No contact was published for this record. The registry link below has the sponsor’s details.

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