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Identification of new quality control indicators for AI assisted colonoscopy

Identification of new quality control indicators for AI assisted colonoscopy

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400081562
Enrollment
Unknown
Registered
2024-03-05
Start date
2023-11-01
Completion date
Unknown
Last updated
2024-03-11

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

Conditions

Colorectal cancer

Interventions

Do not use real-time reminder group(Before and after self-checking phase):Do not use real-time reminder
Using real-time reminder group(Before and after self-checking phase):Using real-time reminder

Sponsors

The First Affiliated Hospital of Army Medical University, PLA
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Stage of research on the correlation between "wall rate" and ADRs; 1.1 Endoscopist: Physicians in the Gastrointestinal Endoscopy Centre of the First Affiliated Hospital of the Army Military Medical University, the Gastrointestinal Endoscopy Centre of Chongqing Municipal People's Hospital, and the Gastrointestinal Endoscopy Centre of Zunyi Honghuagang District People's Hospital are proficient in routine gastrointestinal and gastroenterological diagnostic examinations, and the number of total number of endoscopic consultations by highly qualified physicians is greater than 1,000, and that of total number of consultations by lowly qualified physicians is less than or equal to 1,000. 1.2 Patients: 1) Patients who were proposed to complete electronic colonoscopy at the Gastrointestinal Endoscopy Centre of the First Affiliated Hospital of the Army Military Medical University, the Gastrointestinal Endoscopy Centre of Chongqing People's Hospital, and the Gastrointestinal Endoscopy Centre of Zunyi Honghuagang District People's Hospital during the experimental cycle, with complete intraluminal pictures and video data retained; 2)Age greater than or equal to 18 years old; 3) Voluntarily participated in the study and signed an informed consent form. 2.Before and after self-checking phase 2.1 Endoscopist: Physicians in the Gastrointestinal Endoscopy Centre of the First Affiliated Hospital of the Army Military Medical University, the Gastrointestinal Endoscopy Centre of Chongqing Municipal People's Hospital, and the Gastrointestinal Endoscopy Centre of Zunyi Honghuagang District People's Hospital were proficient in routine Gastrointestinal and Gastroenterological diagnostic examinations, with an ADR of >34% per annum for highly senior endoscopists, and =34% per annum for less senior endoscopists. 2.2 Patients: 1) Patients who were proposed to complete electronic colonoscopy at the Gastrointestinal Endoscopy Centre of the First Affiliated Hospital of the Army Military Medical University, the Gastrointestinal Endoscopy Centre of Chongqing People's Hospital, and the Gastrointestinal Endoscopy Centre of Zunyi Honghuagang District People's Hospital during the experimental cycle, with complete intraluminal pictures and video data retained; 2)Age greater than or equal to 18 years old; 3) Voluntarily participated in the study and signed an informed consent form.

Exclusion criteria

Exclusion criteria: 1.Stage of research on the correlation between "mucosa touch rate" and ADRs; 1.1 Endoscopist: 1) Inability to participate in all phases of the study on the correlation between "mucosa touch rate" and ADR. 2) The number of working cases did not meet the sample size requirements. 1.2 Patients: 1) Age <18 years; 2) Gastrointestinal obstruction; 3) Severe medical illness (American Society of Anaesthesiologists score =3); 4) Repeat admission patients. 2.Before and after self-checking phase 2.1 Endoscopist: 1) Unable to participate in both the pre- and post-control stages of the "mucosa touch rate" self-check. 2) Those who do not fulfil the annual ADR requirement. 2.2 Patients: 1) Age <18 years; 2) Gastrointestinal obstruction; 3) Severe medical illness (American Society of Anaesthesiologists score =3); 4) Repeat admission patients.

Design outcomes

Primary

MeasureTime frame
Mucosa touch rate;

Secondary

MeasureTime frame
Identification rate of ileocecal part;Brightness;Contrast;Rotation angle;

Countries

China

Contacts

Public ContactLei chen

The First Affiliated Hospital of Army Medical University, PLA

chenlei1977603@126.com+86 132 2868 3896

Outcome results

None listed

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