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Upper Gastrointestinal Endoscopy Reporting System in Improving Report Quality

W

Wuhan University

Status

Enrolling

Conditions

Endoscopy, Gastrointestinal
Artificial Intelligence

Study type

Observational

Funder types

Other

Identifiers

NCT05851716
EA-23-006

Details and patient eligibility

About

The goal of this observational study is to evaluate the effectiveness of an AI-based reporting system for upper gastrointestinal endoscopy. The main question it aims to answer is: Whether the AI-based reporting system can improve the completeness of the reports, which are drafted by endoscopists with the AI assistance. Participants will undergo upper gastrointestinal endoscopy examination as routine. The junior endoscopists will draft the report with the assiatance of the AI system. And the senior and expert endoscopists will draft the report using the traditional reporting system without AI assistance.

Enrollment

100 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Aged 18 years
  2. Aim to undergo screening, surveillance, and diagnosis
  3. Undergo sedated EGD
  4. Able to read, understand, and sign informed consent

Exclusion criteria

  1. EGD contraindications
  2. Not suitable for sedated endoscopy after anaesthesia evaluation
  3. Biopsy contraindications
  4. Active upper gastrointestinal bleeding or emergency oesophagogastroduodenoscopy (EGD)
  5. Pregnancy
  6. Upper gastrointestinal surgery or residual stomach
  7. Not suitable for recruitment after investigator evaluation because of other high-risk conditions

Trial contacts and locations

1

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Central trial contact

Honggang Yu, MD

Data sourced from clinicaltrials.gov

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