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I-scan for Adenoma Detection

NCT02811419 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 740

Last updated 2019-05-01

Study results available
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Summary

This study is a randomized controlled trial to determine whether i-scan can improve the detection of conventional adenomas and sessile serrated adenomas/polyps.

Conditions

  • Colorectal Adenomatous Polyps

Interventions

DEVICE

i-scan

examination will be performed with i-scan digital enhancement

DEVICE

standard high-definition white light

examination will be performed with high-definition white light

Sponsors & Collaborators

Principal Investigators

  • Jeffrey K Lee, MD · Primary

Study Design

Allocation
RANDOMIZED
Purpose
DIAGNOSTIC
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
50 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2017-02-01
Primary Completion
2017-12-31
Completion
2018-01-31
FDA Device
Yes

Countries

  • United States

Study Locations

More Related Trials

Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02811419 on ClinicalTrials.gov