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Clinical Trial Summary

A Prospective Randomized Comparison of colonoscopy Adenoma Detection Yield of (i) Standard Colonoscopy (SC), (ii) artificial intelligence (Discovery) aided colonoscopy, and (iii) artificial intelligence (Discovery) and permanently mounted balloon (G-EYE®) aided colonoscopy.


Clinical Trial Description

Multi-center, three-arm, randomized, controlled, open-label study. Total of up to 1320 patients will be randomized, including up to 10% for subject drop-out, 440 to each of the three following arms (groups): Group 1 (1st arm): patients will receive standard colonoscopy (SC) Group 2 (2nd arm): patients will receive colonoscopy aided by the Discovery artificial intelligence software (DC) Group 3 (3rd arm): patients will receive colonoscopy aided by the Discovery artificial intelligence software and the G-EYE® balloon (GDC) The purpose of this study is to compare between the diagnostic yield of Standard Colonoscopy, Discovery aided colonoscopy, and Discovery & G-EYE® aided colonoscopy. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05158725
Study type Interventional
Source Dr. Horst Schmidt Klinik GmbH
Contact Ralf Kiesslich, Prof.
Phone +49 611 43-9002
Email Ralf.Kiesslich@helios-gesundheit.de
Status Recruiting
Phase N/A
Start date November 8, 2021
Completion date June 2022

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