OCT Image Quality Performance Evaluation

Status

Withdrawn

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT02991027

Enrollment

Registered

2016-12-13

Start date

2016-12-14

Completion date

2017-07-02

Last updated

2021-12-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy Eyes

Keywords

no known ocular pathology

Brief summary

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

Detailed 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.

Interventions

DEVICEDRI OCT Triton

DRI OCT Triton using micro-electro-mechanical short cavity tunable laser

Study design

Allocation

Intervention model

SINGLE_GROUP

Primary purpose

DIAGNOSTIC

Masking

NONE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

Yes

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

Design outcomes

Primary

Measure	Time frame
OCT image quality	5 minutes
OCT angiography image quality	5 minutes

Secondary

Measure	Time frame
Full Retinal Thickness	5 minutes

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026