Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Topcon Corporation
Age
22–any
Sex
ALL
Healthy volunteers
Accepted
You may be eligible if
Subjects 22 years of age or older on the date of data collection (retrospective) or informed consent (prospective).
For prospective data collection or missing retrospective data collection, subjects able to understand the written informed consent and willing to participate as evidenced by signing the informed consent.
BCVA 20/40 or better (each eye).
Normal eyes to have normal ocular examination in both eyes
Normal eyes to have IOP ≤ 21 mmHg in both eyes
Pathology eyes to have clinical diagnosis of mild or moderate glaucoma in at least one eye
You may not be if
For prospective or missing retrospective data collection, subjects unable to tolerate ophthalmic testing.
Concomitant diseases known to affect the visual field: history of leukemia, dementia, Parkinson's disease, Alzheimer's disease, stroke, or autoimmune diseases.
History of intraocular surgery (uncomplicated cataract or glaucoma surgeries are accepted)
Ocular findings or history of co-morbidities, including, but not limited to: uveitis, non-glaucomatous optic neuropathy, trauma, retinal detachment, vein or artery occlusions, wet age-related macular degeneration, geographic atrophy, proliferative diabetic retinopathy, vitreous hemorrhage, severe cataract, severe non-proliferative diabetic retinopathy. Controlled diabetes and hypertension participants can be included.
Unreliable VF testing and/or poor-quality OCT scans.
