OCT Image Quality Performance Evaluation

Topcon

Status: Withdrawn

Conditions: Healthy Eyes

Treatments: Device: DRI OCT Triton

Study type: Interventional

Funder types: Industry

Identifiers

NCT02991027

Topcon Tabil-801-2016

Details and patient eligibility

About

To evaluate the image qualities and segmentation performance of Topcon's DRI OCT Triton devices using two light sources.

Full description

To evaluate the image qualities and segmentation performance of Topcon's DRI OCT Triton devices using two light sources with equivalent specifications: the micro-electro-mechanical short cavity tunable laser and the micro-electro-mechanical tunable vertical cavity surface emitting laser.

Sex: All

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria

1. Participants must be at least 18 years of age
2. They must be able to complete all testing (all OCT scans)
3. They must volunteer to be in the study and sign the consent form

Exclusion Criteria

1. Subject with history of ocular disease or ocular pathology
2. Subjects unable to complete all OCT imaging modes

Trial design

Primary purpose: Diagnostic

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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0 participants in 1 patient group

Subjects Presenting With Normal Eyes

Experimental group

Description:

Subjects with no known ocular diseases will be imaged using 2 different light sources using the DRI Triton

Treatment:

Device: DRI OCT Triton

Device: DRI OCT Triton