At a glance
ClinicalIndex Comparison RecordN/ACompleted· 1,000 enrolled
Drug / intervention
G-EYE™ colonoscopy +1 moredevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Prospective Randomized Trial to Compare the Clinical Efficiency (Adenoma Detection Rate) of G-EYE™ HD Colonoscopy With Standard HD Colonoscopy
In Brief
A clinical study evaluating G-EYE™ colonoscopy and Standard Colonoscopy for Adenoma and 2 related conditions. Completed, enrolled 1,000 participants across 15 sites in 8 countries.
Detailed Summary
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
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsAdenoma, Polyps, Colorectal Cancer
CountriesDenmark, Germany, India, Israel, Italy, Netherlands, United Kingdom, United States
Collaborators--
Timeline
N/ACompletedFinished
2014201520162017201820192020202120222023202420252026
First PostedAug 2013
Enrollment StartMay 2014
Primary CompletionSep 2016
TodayJul 2026
First PostedAug 6, 2013
Enrollment StartMay 1, 2014
Primary CompletionSep 1, 2016
TodayJul 2, 2026
Enrollment to primary: 2.3 yearsPosted 12.9 years ago
Interventions
G-EYE™ colonoscopydevice
G-EYE™ colonoscopy
Standard Colonoscopydevice
Standard Colonoscopy