Colorectal tumors
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: This study will include patients who visit the outpatient clinic at Keio University Hospital within approximately two years (March 2028) from the date of authorization from the head of the research institution, are diagnosed with a colorectal tumor, undergo lower gastrointestinal endoscopy using a Fujifilm endoscopic system (ELUXEO 8000 system), and who have given informed consent regarding this study.
Exclusion criteria
Exclusion criteria: - Cases involving minors or those lacking the capacity to consent due to dementia, etc. - Other cases deemed unsuitable for registration by the attending physician - Cases where the research participant refuses to participate in this study after registration.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The difference in color is determined by comparing WLI and ACI in each lesion (including indigo carmine spray images). | — |
Secondary
| Measure | Time frame |
|---|---|
| - Calculate quantitative evaluation of color difference, and analyze its distribution and correlation with lesion characteristics. - Correlation between the presence or absence of color difference and tumor characteristics (e.g., histological type, degree of atypia). - Inter-observer agreement rate regarding color difference determination. - Frequency of color difference occurrence by lesion characteristic. | — |
Countries
Japan
Contacts
Keio University Endoscopy center