Comparing Detection of Standard Colonoscopy, CAD-EYE & Combined CAD-EYE &

Status Recruiting

Clinical Trial Summary

Clinical Trial Description

The purpose of this study is to compare the additional diagnostic yield over Standard Colonoscopy (i.e., the adenoma miss-rate reduction) obtained by performing CADEYE and G-EYE® aided colonoscopy, vs. the additional diagnostic yield over Standard Colonoscopy (i.e., the adenoma miss-rate reduction) obtained by performing CAD-EYE aided colonoscopy. This is a single-center, four-arm dual-tandem, randomized, open-label study intended to compare the additional detection yield beyond standard colonoscopy obtained by performing combined CAD-EYE and G-EYE® high definition colonoscopy vs. the additional detection yield beyond standard colonoscopy obtained by performing CAD-EYE high definition colonoscopy. Consecutive adult subjects who were referred for elective colonoscopy will be asked to enroll into this randomized clinical study if the candidate meets the study inclusion and exclusion criteria ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT05237310
Study type	Interventional
Source	Smart Medical Systems Ltd.
Contact	Ralf Kiesslich, Prof.
Phone	+49 611 43-9002
Email	Ralf.Kiesslich@helios-gesundheit.de
Status	Recruiting
Phase	N/A
Start date	February 2, 2022
Completion date	September 2022

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Comparing Detection of Standard Colonoscopy, CAD-EYE and Combined CAD-EYE and G-EYE® Aided Colonoscopy

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms