Skip to content

Research on upper gastrointestinal endoscopy reporting system based on multimodal large language model

Research on upper gastrointestinal endoscopy reporting system based on multimodal large language model

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400091181
Enrollment
Unknown
Registered
2024-10-22
Start date
2024-10-23
Completion date
Unknown
Last updated
2024-10-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

upper gastrointestinal endoscopy

Interventions

Upper gastrointestinal endoscopy group:None

Sponsors

Renmin Hospital of Wuhan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Patient age = 18 years old; 2. Patients who require upper gastrointestinal endoscopy examination; 3.Patients with enough ability to read, understand, and sign informed consent forms; 4.The researchers believe that the subjects are able to understand the process of this clinical study, willing, able to cooperate, and complete all research procedures.

Exclusion criteria

Exclusion criteria: 1. Have participated in other clinical trials, signed the informed consent form and within the follow-up period of other clinical trials; 2. High-risk diseases or other special circumstances that the investigator believes are not suitable for the subject to participate in the clinical trial; 3. Pregnant or lactating women; 4. Drug or alcohol abuse or mental illness in the past 5 years; 5. Known acute phase of esophageal, gastric, duodenal perforation; 6. Known acute severe throat disease that is unable to enter the scope; 7. Acute phase of known corrosive esophageal injury; 8. Cellulitis gastritis; 9. Those who are mentally disturbed and unable to cooperate; 10. Patients with high spinal curvature deformity; 11. Those with insufficiency of important organs such as heart and lungs; 12. Uncontrolled hypertension; 13. Patients who are unable to cooperate with the completion of gastroscopy due to other reasons.

Design outcomes

Primary

MeasureTime frame
Integrity of lesion report;

Secondary

MeasureTime frame
Completeness of lesion feature description;Report generation time;Report overall satisfaction score;

Countries

China

Contacts

Public ContactHonggang Yu

Renmin Hospital of Wuhan University

yuhonggang1968@163.com+86 138 7128 1899

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026