Glaucoma
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Glaucoma patients between ages 50 and 75, who visit the Ophthalmology clinic at University Medical Center Groningen, that have provided the informed consent form and meet the inclusion-exclusion criteria. Healthy subjects between ages 50 and 75, who have provided the informed consent form and returned the questionnaire with results which do not indicate ophthalmic abnormalities.
Exclusion criteria
Exclusion criteria: Glaucoma Patients: Visual acuity less than 0.8 Non-glaucomatous visual field loss;Healthy Subjects: Visual acuity less than 0.8 Any visual field loss Intraocular pressure above 21 mmHg Positive family history of glaucoma
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Contrast gain control as a function of the frequence in which background luminance changes in time. Contrast sensitivity in central and peripheral sites of the retina will be measured by using a staircase method. The contrast gain control will be defined as the difference between the contrast sensitivity measured at static (0 Hz) versus the dynamic light conditions. The contrast gain control can then be compared between the healthy control group and glaucoma patients. We measure contrast gain control at two different values of the mean background luminance and for two polarities (white (increment) and black (decrement) stimuli on a gray background). | — |
Secondary
| Measure | Time frame |
|---|---|
| Critical Fusion Frequency (CFF). CFF is the highest frequency at which flicker can be detected. This will be measured in the central and peripheral visual field for a range of background luminances. | — |
Countries
Netherlands