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Prospective Randomized Controlled Trial of High-Definition White-light Colonoscopy Versus High-Definition White-light Colonoscopy With Endocuff Vision for Endpoints of Procedural Times
This study seeks to compare colonoscopy results between a standard method and one using a distal scope attachment (Endocuff Vision).
For this study, subjects will be randomized into one of two groups (those who receive a standard colonoscopy and those who receive a colonoscopy with an Endocuff Vision attachment). Results will then be compared between the two; these include insertion time (time it takes to reach the cecum of the large intestine), inspection time (time spent examining the large intestine), the total time per each polypectomy (removal of polyps in the colon), and the total procedure time of the colonoscopy.
Age
40 - No limit years
Sex
ALL
Healthy Volunteers
Yes
Indiana University
Indianapolis, Indiana, United States
Start Date
December 11, 2017
Primary Completion Date
April 18, 2018
Completion Date
April 18, 2018
Last Updated
August 6, 2019
200
ACTUAL participants
Endocuff Vision
DEVICE
Lead Sponsor
Indiana University
NCT04704661
NCT04674267
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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