OCT Image Quality Performance Evaluation

Not Applicable

Withdrawn

• Conditions: Healthy Eyes
• Interventions: Device: DRI OCT Triton

• Registration Number: NCT02991027
• Lead Sponsor: Topcon Medical Systems, Inc.

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.

Study Timeline

• Study First Submitted: 2016-12-09
• Study First Submitted QC: 2016-12-09
• Study First Posted: 2016-12-13
• Study Start: 2016-12-14
• Primary Completion: 2017-06-12
• Study Completion: 2017-07-02
• Status Verified: 2021-10
• Last Update Submitted: 2021-12-10
• Last Update Posted: 2021-12-16

Recruitment & Eligibility

• Status: WITHDRAWN
• Sex: All
• Target Recruitment: Not specified

Inclusion Criteria

Not provided

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Exclusion Criteria

Not provided

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Subjects Presenting With Normal Eyes	DRI OCT Triton	Subjects with no known ocular diseases will be imaged using 2 different light sources using the DRI Triton

Primary Outcome Measures

Name	Time	Method
OCT image quality	5 minutes
OCT angiography image quality	5 minutes

Secondary Outcome Measures

Name	Time	Method
Full Retinal Thickness	5 minutes

Trial Locations

Locations (1)

Topcon Medical Systems Inc.; 🇺🇸 Oakland, New Jersey, United States