Colorectal Cancer Clinical Trial
Official title:
Prospective Randomized Trial to Compare the Clinical Efficiency (Adenoma Detection Rate) of G-EYE™ HD Colonoscopy With Standard HD Colonoscopy
The purpose of this study is to compare the adenoma detection rate of G-EYE™ high definition colonoscopy with that of standard high definition colonoscopy
This is a multicenter, two-arm, randomized, open-label study intended to compare the
detection rate obtained by performing G-EYE™ high definition colonoscopy vs. the detection
rate obtained by performing high definition standard colonoscopy.
The study will enroll 1000 subjects. 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.
Subjects will sign informed consent form and undergo randomization. The study includes a
run-in preliminary phase of 270 patients to allow physicians to get familiar with the G-EYE™
endoscope.
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