Evaluation of the Precision of the Microperimetry Function of the Spectral OCT/SLO
Status: | Completed |
---|---|
Conditions: | Cardiology, Ocular, Diabetes |
Therapuetic Areas: | Cardiology / Vascular Diseases, Endocrinology, Ophthalmology |
Healthy: | No |
Age Range: | 21 - Any |
Updated: | 4/21/2016 |
Start Date: | October 2012 |
End Date: | November 2012 |
To conduct a precision study to assess the microperimetry function of the Spectral OCT/SLO.
The study will assess variability across measurements taken by three different
operator-device configuration across clinical sites, variability between subjects within a
given operator-device configuration, and variability within a subject for a single
operator-device configuration.
The study will assess variability across measurements taken by three different
operator-device configuration across clinical sites, variability between subjects within a
given operator-device configuration, and variability within a subject for a single
operator-device configuration.
Inclusion Criteria:
- Subject must be 21 years of age or older.
- Subjects recruited to Cohort 1 will have no known retinal disease except for
refractive errors (-7.5 D to +7.5 diopters).Subjects who are recruited to Cohort 2
will have one or more of the following retinal pathologies: early and intermediate
Age-Related Macular Degeneration, Geographic Atrophy, Diabetic Retinopathy (mild,
moderate, severe), Macular Edema secondary to Diabetes, Retinal Vein Occlusion,
Central Serous Retinopathy, Pattern Dystrophy, Epiretinal Membrane or Macular Hole.
- Subjects who have signed an informed consent form.
- Subjects who can comply with the protocol.
Exclusion Criteria:
- Subjects younger than 21 years of age.
- Subjects who cannot comply with the protocol.
- Subjects who cannot complete the Simple Test procedures
- Subjects who are not available to be testing 3 times during the day (Morning, Mid -
Day, and Afternoon).
- Subjects with visual acuity worse than 20/100 (Best Corrected).
- Subjects with dense media opacities.
- Ocular surgery anticipated on the day of the study visit.
We found this trial at
3
sites
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