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This study investigates a new technology to assess the structure and function inside the eye. Retinal imaging of subjects with inner and outer retinal defects to detect areas of abnormal structure and function compared to other visual function tests.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Laser Speckle Blood Flow Group | Experimental |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| LSFG-NAVI | Device | laser-speckle blood flow of ocular arteries and veins |
|
| Measure | Description | Time Frame |
|---|---|---|
| Ocular Blood Flow | imaging the movement of blood through blood vessels in retina and optic nerve | 1 day |
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Controls:
Inclusion:
Normal eye exam in last 2 years
Exclusion:
Cataract or media opacity that would degrade the imaging of the retina. Mild cataracts are okay. Any abnormalities of the retina or optic nerve that could affect metabolism of the retina outside of normal.
Subjects with Inner Retina Defect:
Inclusion:
Defined structural defect to include those with Ischemic optic neuropathy, branch retinal artery occlusion (BRAO), hemianopia or visual field defect that respects the vertical meridian, inherited mitochondrial optic neuropathies such as Leber's and Dominant Optic Neuropathy, other retinopathies or optic neuropathies.
Exclusion:
Cataract or media opacity that would degrade the imaging of the retina. Mild cataracts are okay.
Subjects with Outer Retinal Defect:
Inclusion:
AZOOR (acute zonal occult outer retinopathy) or other focal or diffuse outer photoreceptor loss of function
Exclusion:
Cataract or media opacity that would degrade the imaging of the retina. Mild cataracts are okay.
The 450 total is to allow for exclusion of some subjects or in the event that the enrolled subject blinks too much or cannot fixate on a visual target adequately to maintain the same eye position during the short imaging interval. We hope to have a total of 450 (50 controls and 400 patients)
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Julie K Nellis, BSN | Contact | 319-356-8299 | julie-nellis@uiowa.edu | |
| Jan M Full, BSN | Contact | 319-356-8299 | jan-full@uiowa.edu |
| Name | Affiliation | Role |
|---|---|---|
| Randy H Kardon, MD, PhD | University of Iowa Department of Ophthalmology | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| University of Iowa Department of Ophthalmology | Recruiting | Iowa City | Iowa | 52242 | United States |
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| ID | Term |
|---|---|
| D018917 | Optic Neuropathy, Ischemic |
| D015356 | Retinal Artery Occlusion |
| D006423 | Hemianopsia |
| D029242 | Optic Atrophy, Hereditary, Leber |
| C538223 | Acute zonal occult outer retinopathy |
| D009901 | Optic Nerve Diseases |
| D012164 | Retinal Diseases |
| ID | Term |
|---|---|
| D003389 | Cranial Nerve Diseases |
| D009422 | Nervous System Diseases |
| D005128 | Eye Diseases |
| D014652 | Vascular Diseases |
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| D002318 |
| Cardiovascular Diseases |
| D001157 | Arterial Occlusive Diseases |
| D014786 | Vision Disorders |
| D012678 | Sensation Disorders |
| D009461 | Neurologic Manifestations |
| D001766 | Blindness |
| D012816 | Signs and Symptoms |
| D013568 | Pathological Conditions, Signs and Symptoms |
| D015418 | Optic Atrophies, Hereditary |
| D009896 | Optic Atrophy |
| D020271 | Heredodegenerative Disorders, Nervous System |
| D019636 | Neurodegenerative Diseases |
| D015785 | Eye Diseases, Hereditary |
| D030342 | Genetic Diseases, Inborn |
| D009358 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| D028361 | Mitochondrial Diseases |
| D008659 | Metabolic Diseases |
| D009750 | Nutritional and Metabolic Diseases |