None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Male or female adults aged 50 to 80 years undergoing colonoscopy for screening indications Patients who provided informed consent for study participation
Exclusion criteria
Exclusion criteria: 1.History of colorectal resection 2.History of inflammatory bowel disease 3.History of hereditary intestinal diseases such as polyposis syndrome 4.Patients unable to undergo polypectomy or biopsy (e.g., continuous use of anticoagulants) 5.Patients who do not consent to participate in the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Right-sided Colon Adenoma Detection Rate (RC-ADR) | — |
Secondary
| Measure | Time frame |
|---|---|
| ight-sided Colon Adenoma and Serrated Lesion Detection Rate (RC-ASDR);Right-sided Colon Serrated Lesion Detection Rate (RC-SDR);Number and characteristics of lesions additionally detected only during the Second Forward-View (SFV) examination;Incidence of procedure-related adverse events (perforation, bleeding, etc.);Comparison of right-sided adenoma detection rates according to the endoscopist's experience (Expert vs. Trainee);Mean Adenoma per Patient (MAP);Learning curve analysis: Comparison of ADR in TXI mode between the early and late phases of the study;Rate of change in the recommended surveillance interval based on the second-look findings | — |
Countries
Korea, Republic of
Contacts
Soonchunhyang University Hospital Bucheon