Use of Accessory Device AmplifEYE During Average Risk Screening

Clinical Trial Summary

The purpose of this investigator-initiated study is to determine whether the use of an accessory device called AmplifEYE can improve colonoscopy quality in patients who are undergoing average risk colorectal cancer screening. Primary end point is adenoma detection rates.

See also
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NCT number	NCT02885987
Study type	Interventional
Source	Loma Linda University
Contact
Status	Withdrawn
Phase	N/A
Start date	August 3, 2017
Completion date	March 2022

Use of Accessory Device AmplifEYE During Average Risk Screening Colonoscopy to Increase Adenoma Detection Rate

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms