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Endocuff Vision Colonoscopy vs. AmplifEYE Colonoscopy

NCT03560128 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 634

Last updated 2019-10-08

Study results available
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Summary

The study aims to compare the results between colonoscopies with two different attachments on the distal end of the colonoscope.

Conditions

Interventions

DEVICE

Endocuff Vision device

Subjects randomized to undergo a colonoscopy procedure with the Endocuff Vision device will have this device placed on the colonoscope used during their procedure.

DEVICE

AmplifEYE device

Subjects randomized to undergo a colonoscopy procedure with the AmplifEYE device will have this device placed on the colonoscope used during their procedure.

Sponsors & Collaborators

  • Indiana University

    lead OTHER

Principal Investigators

  • Douglas K Rex, MD · Indiana University

Study Design

Allocation
RANDOMIZED
Purpose
SCREENING
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
40 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2018-04-12
Primary Completion
2018-12-18
Completion
2018-12-18
FDA Device
Yes

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

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 NCT03560128 on ClinicalTrials.gov