Prospective Trial to Compare ADR of G-EYE™ Colonoscopy With Standard Colonoscopy

NCT02545699 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 350

Last updated 2016-06-07

No results posted yet for this study

Summary

The purpose of this study is to compare the adenoma detection rate (ADR) of the G-EYE™ colonoscopy with that of standard colonoscopy.

Conditions

Interventions

DEVICE

G-EYE™ Colonoscopy

G-EYE™ Colonoscopy

DEVICE

Standard Colonoscopy

Standard Colonoscopy

Sponsors & Collaborators

  • Smart Medical Systems Ltd.

    lead INDUSTRY

Principal Investigators

  • Tova Rainis, Dr. · Bnai Zion Medical Center

Study Design

Allocation
RANDOMIZED
Purpose
DIAGNOSTIC
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
50 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2015-09-30
Primary Completion
2017-06-30
Completion
2017-06-30

Countries

  • Israel

Study Locations

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Entities

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 NCT02545699 on ClinicalTrials.gov