colonic polyps
Conditions
Interventions
Group undergoing routine lower gastrointestinal endoscopy with AI
Group undergoing routine lower gastrointestinal endoscopy without AI
Sponsors
Tobata Kyoritsu Hospital
Saga University Hospital, Fukuoka University Chikushi Hospital, University of Miyazaki Hospital, University of the Ryukyus Hospital, Kyushu University Hospital, Kumamoto University Hospital, Kagoshima University Hospital, Hospital of the University of Occupational and Environmental Health, Oita University Hospital
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Patients scheduled for routine lower gastrointestinal endoscopy Patients who have received a full explanation of the situation from the attending physician regarding the contents of this study and have obtained consent
Exclusion criteria
Exclusion criteria: Patients with a history of colorectal resection Patients with inadequate observation due to poor pretreatment Patients with inflammatory bowel disease, familial adenomatous colorectal adenomatosis, or other polyposis Patients with difficulty in deep insertion Cases of gastrointestinal bleeding requiring endoscopic hemostasis Other cases judged by the examiner to be unsuitable for a safe examination method Cases in which consent for the study cannot be obtained.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| MAP (mean number of adenoma per procedure) between the two AI and non-AI groups | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. MAP and MPP (mean polyps detected per procedure) in the state of excessive fatigue 2. MAP and MPP under high stress conditions 3. MAP and MPP in over-fatigued and high-stress conditions 4. consideration of ADR and PDR 5. Examination of changes in fatigue and stress levels before and after the test 6. Examination by years of experience of the practitioner 7. examination time | — |
Countries
Japan
Contacts
Public ContactKensei Ohtsu
Tobata Kyoritsu Hospital Department of gastroenterology
Outcome results
None listed