Triton Fundus Autofluorescence and Fluorescein Angiography

NCT ID: NCT03107104

Last Updated: 2022-06-08

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

47 participants

Study Classification

OBSERVATIONAL

Study Start Date

2017-03-30

Study Completion Date

2017-09-30

Brief Summary

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Compare the image quality of the fundus autofluorescence and fluorescein angiography

Detailed Description

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The objectives of this study are to:

1. Compare the image quality of the fundus autofluorescence (FAF) photographs between DRI OCT Triton (plus) and TRC-50DX retinal camera.
2. Compare the image quality of the fluorescein angiography (FA) photographs between DRI OCT Triton (plus) and TRC-50DX retinal camera.

Conditions

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Medical Need for Fluorescein Angiography Imaging

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Medical need for FA imaging

Subjects deemed to have a medical need for FA imaging will be imaged on the Topcon DRI OCT Triton (plus) and TRC-50DX retinal camera

Topcon DRI OCT Triton (plus)

Intervention Type DEVICE

The Topcon DRI OCT Triton (plus) is an OCT with a fundus camera used for diagnostic purposes

TRC-50DX retinal camera

Intervention Type DEVICE

The TRC-50DX retinal camera is a fundus camera used for diagnostic purposes

Interventions

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Topcon DRI OCT Triton (plus)

The Topcon DRI OCT Triton (plus) is an OCT with a fundus camera used for diagnostic purposes

Intervention Type DEVICE

TRC-50DX retinal camera

The TRC-50DX retinal camera is a fundus camera used for diagnostic purposes

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

1. Subjects must be at least 18 years of age
2. Subjects able to understand the written informed consent and willing to participate as evidenced by signing the informed consent
3. Subjects who consent to, via clinic's standard FA consent form, and will undergo dye injection for FA imaging at the clinic visit based on medical need

Exclusion Criteria

1. Subjects unable to tolerate ophthalmic imaging
2. Subjects with ocular media not sufficiently clear to obtain acceptable fundus images
3. Patients with ocular motility dysfunction
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Topcon Medical Systems, Inc.

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Charles Riesman, MS

Role: STUDY_CHAIR

Topcon Corporation

Locations

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Vitreous Retina Macula Consultants of New York

New York, New York, United States

Site Status

Countries

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United States

Other Identifiers

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Triton FA FAF

Identifier Type: -

Identifier Source: org_study_id

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