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Clinical Study of the Optic Disc Parameters

NCT02277119 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 109

Last updated 2022-06-28

Study results available
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Summary

Assess the repeatability and agreement of the Optic Disc Parameters, Retinal Nerve Fiber Layer (RNFL) Thickness, and Full Retinal Thickness between the Maestro and iVue OCT devices

Conditions

  • Normal Healthy Subjects With No Known Ocular Diseases
  • Glaucomatous Eyes
  • Eyes With Retinal Diseases

Interventions

DEVICE

Maestro

OCT machines used for diagnostic purposes

DEVICE

iVue

OCT machines used for diagnostic purposes

Sponsors & Collaborators

  • Topcon Medical Systems, Inc.

    lead INDUSTRY

Principal Investigators

  • Mike Sinai, PhD · Topcon Corporation

Study Design

Allocation
RANDOMIZED
Purpose
DIAGNOSTIC
Masking
SINGLE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2014-10-31
Primary Completion
2015-01-31
Completion
2015-02-28

Countries

  • United States

Study Locations

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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 NCT02277119 on ClinicalTrials.gov