Clinical Trials Directory

Trials / Completed

CompletedNCT02277119

Clinical Study of the Optic Disc Parameters

Topcon 3D OCT-1 Maestro Optic Disc and RNFL Study: Agreement and Repeatability Comparison With the iVue

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
109 (actual)
Sponsor
Topcon Medical Systems, Inc. · Industry
Sex
All
Age
18 Years
Healthy volunteers
Accepted

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

Interventions

TypeNameDescription
DEVICEMaestroOCT machines used for diagnostic purposes
DEVICEiVueOCT machines used for diagnostic purposes

Timeline

Start date
2014-10-01
Primary completion
2015-01-01
Completion
2015-02-01
First posted
2014-10-28
Last updated
2022-06-28
Results posted
2016-11-02

Locations

2 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT02277119. Inclusion in this directory is not an endorsement.