Triton Fundus Autofluorescence and Fluorescein Angiography

Topcon

Status: Completed

Conditions: Medical Need for Fluorescein Angiography Imaging

Treatments: Device: Topcon DRI OCT Triton (plus); Device: TRC-50DX retinal camera

Study type: Observational

Funder types: Industry

Identifiers

NCT03107104

Triton FA FAF

Details and patient eligibility

About

Compare the image quality of the fundus autofluorescence and fluorescein angiography

Full description

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.

Enrollment: 47 patients

Sex: All

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion and exclusion criteria

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

Trial design

47 participants in 1 patient group

Medical need for FA imaging

Description:

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

Treatment:

Device: Topcon DRI OCT Triton (plus)

Device: TRC-50DX retinal camera