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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03475173
Other study ID # 201611825
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date May 6, 2019
Est. completion date March 1, 2028

Study information

Verified date May 2024
Source University of Iowa
Contact Julie K Nellis, BSN
Phone 319-356-8299
Email julie-nellis@uiowa.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Recruitment information / eligibility

Status Recruiting
Enrollment 500
Est. completion date March 1, 2028
Est. primary completion date January 1, 2028
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 99 Years
Eligibility 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)

Study Design


Intervention

Device:
LSFG-NAVI
laser-speckle blood flow of ocular arteries and veins

Locations

Country Name City State
United States University of Iowa Department of Ophthalmology Iowa City Iowa

Sponsors (1)

Lead Sponsor Collaborator
Randy Kardon

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Ocular Blood Flow imaging the movement of blood through blood vessels in retina and optic nerve 1 day
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