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EndoRings Colonoscopy vs Standard Colonoscopy

NCT03418662 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 592

Last updated 2019-09-20

Study results available
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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.

Conditions

Interventions

DEVICE

EndoRings device

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.

Sponsors & Collaborators

  • US Endoscopy

    collaborator INDUSTRY

  • Indiana University

    lead OTHER

Principal Investigators

  • Douglas K Rex, MD · Indiana University

Study Design

Allocation
RANDOMIZED
Purpose
SCREENING
Masking
NONE
Model
PARALLEL

Eligibility

Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2018-01-19
Primary Completion
2018-09-13
Completion
2018-09-13
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 NCT03418662 on ClinicalTrials.gov