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Completed

NCT Number: NCT06969794

Single-center, Randomized, Superiority Pivotal Clinical Study to Evaluate the Efficacy of Artificial Intelligence-based Upper Gastrointestinal Endoscopy Image

We will conduct a single-center retrospective study at a university hospital. A total of 3,385 gastroscopic white-light images from patients with pathologically confirmed findings will be analyzed. The AI software will automatically identify images as non-neoplastic or neoplastic (low-grade dysplasia, high-grade dysplasia, early gastric cancer with mucosal or submucosal invasion, or advanced gastric cancer) and highlighted lesion locations. Two experienced endoscopists will independently review the same image set without AI assistance for comparison. Primary outcomes are sensitivity and specificity of the AI in detecting gastric neoplasms (by category and overall), and the localization accuracy measured by the localization receiver operating characteristic (LROC) curve area. Secondary outcomes is includes comparison of the AI's diagnostic performance with that of endoscopists.

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Key information

Age range

20 year–100 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Chuncheon Sacred Heart hospital

Chuncheon, Gangwon-do, 24253, South Korea

About this study

We will conduct a single-center retrospective study at a university hospital. A total of 3,385 gastroscopic white-light images from patients with pathologically confirmed findings will be analyzed. The AI software will automatically identify images as non-neoplastic or neoplastic (low-grade dysplasia, high-grade dysplasia, early gastric cancer with mucosal or submucosal invasion, or advanced gastric cancer) and highlighted lesion locations. Two experienced endoscopists will independently review the same image set without AI assistance for comparison. Primary outcomes are sensitivity and specificity of the AI in detecting gastric neoplasms (by category and overall), and the localization accuracy measured by the localization receiver operating characteristic (LROC) curve area. Secondary outcomes is includes comparison of the AI's diagnostic performance with that of endoscopists.

Inclusion criteria

Age 19 or older At least one gastric lesion biopsied with a definitive pathological diagnosis Availability of high-quality white-light endoscopy images of the lesion and surrounding mucosa

Exclusion criteria

Poor-quality images (e.g., out of focus or obscured) Lack of histopathological confirmation of the lesion

Each image will be paired with a reference standard diagnosis based on the pathology result for that lesion or region.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age 19 or older
  • At least one gastric lesion biopsied with a definitive pathological diagnosis
  • Availability of high-quality white-light endoscopy images of the lesion and surrounding mucosa

Exclusion criteria

  • Poor-quality images (e.g., out of focus or obscured)
  • Lack of histopathological confirmation of the lesion

Treatment and study plan

Primary outcomes

  1. AI performance

    Time frame: Day 1

    sensitivity and specificity of the AI in detecting gastric neoplasms (by category and overall), and the localization accuracy measured by the localization receiver operating characteristic (LROC) curve area.

Secondary outcomes

  1. comparison of the AI's diagnostic performance with that of endoscopists.

    Time frame: Day 1

    Secondary outcomes included comparison of the AI's diagnostic performance with that of endoscopists. (sensitivity and specificity of the AI in detecting gastric neoplasms (by category and overall), and the localization accuracy measured by the localization receiver operating characteristic (LROC) curve area.)

Sponsors and collaborators

Lead sponsor

Chuncheon Sacred Heart Hospital

Other

Registry information

Official study title

Single-center, Single Group, Randomized, Superiority Pivotal Clinical Study to Evaluate the Efficacy and Safety of Artificial Intelligence-based Upper Gastrointestinal Endoscopy Image Diagnosis Aid Software

Important dates

Study start
2023
Primary completion
2023
Study completion
2023
First posted
May 14, 2025
Registry last updated
May 14, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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