D12.6 K63.5
Conditions
Interventions
Group 1: Study Procedure
This is a prospective, multicenter, randomized real-world study designed to evaluate the impact of a commercially available artificial intelligence (AI)-based computer-assiste
Sponsors
Universitätsklinikum Schleswig-Holstein Campus Kiel
Eligibility
Sex/Gender
All
Age
18 Years to 85 Years
Inclusion criteria
Inclusion criteria: - Indication für screening colonoscopy - Age > 18 years - Sufficient knowledge of German - written informed consent
Exclusion criteria
Exclusion criteria: - Participation in this study at an earlier time point - Emergency endoscopy - prior screening colonoscopy < 3 years
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Endpoint: Polyp detection rate When will the endpoint evaluated: Immediately during screening colonoscopy. How will the endpoint be evaluated: endoscopically by screening colonoscopy. | — |
Secondary
| Measure | Time frame |
|---|---|
| Adenoma detection rate Polyp size and localisation Polyp differentiation Histology of polyps Rate of colorectal cancer Complication rate Quality of bowel prepration Time of endoscopy (i.e. withdrawal) | — |
Countries
Germany
Contacts
Public ContactMark Ellrichmann
Interdisziplinäre EndoskopieUniversitätsklinikum Schleswig-Holstein, Campus Kiel
Outcome results
None listed