Retina Disease
Conditions
Brief summary
Images will be collected on the modified P200TE
Interventions
DEVICEimaging device
images captured on a modified P200TE
Sponsors
Optos, PLC
Study design
Observational model
OTHER
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
22 Years to No maximum
Healthy volunteers
Yes
Inclusion criteria
Male or female participants 22 years of age or older who have full legal capacity to volunteer on the date the informed consent is signed Participants who can follow the instructions by the clinical staff at the clinical site Participants who agree to participate in the study Participants with posterior segment eye disease. Example of pathologies may include but are not limited to Age-related macular degeneration, glaucoma, diabetic retinopathy, posterior uveitis, central serous chorioretinopathy, vein occlusion, epiretinal membrane and others as confirmed by the investigator.
Exclusion criteria
Participants unable to tolerate ophthalmic imaging. Participants with ocular media not sufficiently clear to obtain acceptable images. Unable to obtain acceptable image quality on participant.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Number of images | 1 year |
Countries
United States
Outcome results
None listed