Colorectal Cancer Clinical Trial
Official title:
Prospective Randomized Trial to Compare the Adenoma Detection Rate of G-EYE™ Colonoscopy With Standard Colonoscopy
The purpose of this study is to compare the adenoma detection rate (ADR) of the G-EYE™ colonoscopy with that of standard colonoscopy.
This is a single-center, two-arm , randomized, open-label study intended to compare the
detection rate obtained by performing G-EYE™ colonoscopy vs. the detection rate obtained by
performing standard colonoscopy.
The study will enroll 350 subjects. Consecutive adult subjects who were referred for
elective colonoscopy will be asked to enroll in this randomized clinical study if the
candidate meets the study inclusion and exclusion criteria.
Subjects will sign an informed consent form and undergo randomization.
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Diagnostic
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