At a glance
ClinicalIndex Comparison RecordN/ACompleted· 592 enrolled
Drug / intervention
EndoRings devicedevice
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.
A Randomized Trial Comparing the Adenoma Detection Rates Between EndoRings Colonoscopy (EC) and Standard Colonoscopy (SC).
In Brief
A clinical study evaluating EndoRings device for Colorectal Adenoma and 2 related conditions. Completed, enrolled 592 participants across 1 site.
Detailed Summary
The study aims to compare the results between a standard colonoscopy to a colonoscopy with an attachment on the distal end of the colonoscope.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsColorectal Adenoma, Colorectal Polyp, Colon Cancer
CountriesUnited States
CollaboratorsUS Endoscopy
Timeline
N/ACompletedFinished
201820192020202120222023202420252026
Enrollment StartJan 2018
First PostedFeb 2018
Primary CompletionSep 2018
TodayJul 2026
First PostedFeb 1, 2018
Enrollment StartJan 19, 2018
Primary CompletionSep 13, 2018
TodayJul 2, 2026
Enrollment to primary: 8 monthsPosted 8.4 years ago
Interventions
EndoRings devicedevice
Subjects randomized to undergo a colonoscopy procedure with the EndoRings device will have the device placed on the colonoscope that will be used during their procedure.