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Prospective Trial to Compare the Clinical Efficiency of G-EYE™ HD Colonoscopy With Standard HD Colonoscopy

NCT01917513 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 1000

Last updated 2018-01-23

Study results available
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Summary

The purpose of this study is to compare the adenoma detection rate of G-EYE™ high definition colonoscopy with that of standard high definition 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

  • Ralf Kiesslich, Prof. · Helios Dr. Horst Schmidt Kliniken, Wiesbaden, Germany

Study Design

Allocation
RANDOMIZED
Purpose
DIAGNOSTIC
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
50 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2014-05-31
Primary Completion
2016-09-30
Completion
2016-09-30

Countries

  • United States
  • Denmark
  • Germany
  • India
  • Israel
  • Italy
  • Netherlands
  • United Kingdom

Study Locations

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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 NCT01917513 on ClinicalTrials.gov