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Not yet recruiting NCT07208864

Efficacy of an AI System in Training Endoscopists to Assess Gastric Intestinal Metaplasia Via the EGGIM Score

No phase Interventional Gastric Intestinal Metaplasia

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: AI-assisted EGGIM scoring, Conventional EGGIM scoring.
Who it may be relevant to
Registry conditions: Gastric Intestinal Metaplasia. Basic parameters: No limits · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
China
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Efficacy of an AI System in Training Endoscopists to Assess Gastric Intestinal Metaplasia Via the EGGIM Score: A Randomized Controlled Trial

Overview

This prospective randomized controlled trial with a crossover design incorporated image-enhanced endoscopy (IEE) videos demonstrating complete standardized examinations of five standard gastric areas (antrum greater curvature, antrum lesser curvature, incisura, corpus lesser curvature, and corpus greater curvature). Endoscopists were stratified by experience level and randomly assigned to either the AI-assisted scoring first group, which performed EGGIM scoring with AI assistance in the initial phase followed by conventional scoring after a washout period, or the conventional scoring first group, which completed the assessments in reverse order. The study primarily evaluated the training efficacy of the EGGIM-AI system for improving endoscopists' EGGIM scoring performance by comparing diagnostic accuracy metrics including the area under the receiver operating characteristic curve (AUC), sensitivity, and specificity between groups at different study phases, with histopathological results serving as the gold standard.

Interventions

  • Diagnostic test AI-assisted EGGIM scoring
    Endoscopists will evaluate the videos with the assistance of the AI system via EGGIM score.
  • Diagnostic test Conventional EGGIM scoring
    Endoscopists will evaluate the videos without the assistance of the AI system via EGGIM score.

Primary outcome measures

  • Efficacy of the EGGIM-AI system for improving endoscopists' EGGIM scoring performance [Time frame: Through study completion, an average of 3 months]
Secondary outcome measures (1)
  • Performance of EGGIM scoring by endoscopists with varying experience levels [Time frame: Through study completion, an average of 3 months]

Eligibility criteria

Inclusion criteria

Endoscopists who have performed ≥50 image-enhanced endoscopy (IEE) procedures per year and demonstrated competency in performing standardized IEE.

Exclusion criteria

Endoscopists who participated in data acquisition or were unblinded to patients' identifiable information and clinical data.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Crossover
Masking
Single blind
Primary purpose
Diagnostic

Study locations

China · 1 center
  • Qilu Hospital of Shandong University — Jinan

Identifiers

NCT: NCT07208864 · 2025SDU-QILU-4

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗