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Performance Evaluation of the NaviAid™ G-Eye System

NCT01552200 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 126

Last updated 2014-04-08

No results posted yet for this study

Summary

The purpose of this study is to compare the additional diagnostic yield obtained by performing NaviAid™ G-Eye procedure vs. the diagnostic yield obtained by performing standard colonoscopy procedure.

Conditions

Interventions

PROCEDURE

Group A-Standard Colonoscopy, then NaviAid™ G-Eye procedure

Standard Colonoscopy,NaviAid™ G-Eye procedure

PROCEDURE

Group B-NaviAid™ G-Eye procedure, then Standard Colonoscopy

G-Eye procedure, Standard Colonoscopy

Sponsors & Collaborators

  • Smart Medical Systems Ltd.

    lead INDUSTRY

Principal Investigators

  • Erwin Santo, MD · Tel-Aviv Sourasky Medical Center

  • Beny Shpak, MD · Laniado Hospital

  • Yael Kopelman, MD · Hadassah Medical Organization

Study Design

Allocation
RANDOMIZED
Purpose
DIAGNOSTIC
Masking
NONE
Model
CROSSOVER

Eligibility

Min Age
40 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2012-06-30
Primary Completion
2013-06-30
Completion
2013-06-30

Countries

  • Germany
  • Israel

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 NCT01552200 on ClinicalTrials.gov