Evaluation of the Precision of the Microperimetry Function of the Spectral OCT/SLO
Completed
Conditions studied: Age-Related Macular Degeneration, Geographic Atrophy, Diabetic Retinopathy, Macular Edema, Retinal Vein Occlusion, Central Serous Retinopathy, Pattern Dystrophy of Macula, Epiretinal Membrane, Macular Hole
In brief
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.
Key facts
- Study ID
- NCT01692938
- Run by
- Optos, PLC
- People needed
- 32
- Starts
- 2012-10-01
- Expected to finish
- 2012-11-01
- Last updated by the study team
- 2017-05-10
Who can join
Age: 21 and older. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- 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.
You may not qualify if…
- 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.
Where it is running
- Retina Group of Florida — Fort Lauderdale, Florida, United States
- Johns Hopkins Unversity — Baltimore, Maryland, United States
- Valley Retina Institute — McAllen, Texas, United States
Full record on ClinicalTrials.gov
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