Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
50 participants
OBSERVATIONAL
2012-06-30
2012-12-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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CASE_CONTROL
RETROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
* Age 40 years or older
* ETDRS best corrected visual acuity better than 5 letters
* History of Dry Age Relted Macular Degeneration; Retinitis Pigmentosa; Stargardt's disease
* No Anti-VEGF treatments for at least 3 months prior to study
* No new antioxidant/vitamin supplementation for at least 3 months prior to study
Exclusion Criteria
* Significant media opacities (exclude NS 4+) that may interfere with assessing visual acuity
* Presence of pigment epithelial tears or rips
* Known serious allergies to fluorescein dye
* Presence of retinal neovascularization
* Any treatment with an investigation agent in the past 30 days
50 Years
ALL
Yes
Sponsors
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Retina Institute of Hawaii
OTHER
Responsible Party
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Principal Investigators
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George Papastergiou, MD
Role: PRINCIPAL_INVESTIGATOR
Retina Institute of Hawaii
Locations
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Hawaii Cataract Laser Institute - Hilo
Hilo, Hawaii, United States
Retina Institute of Hawaii
Honolulu, Hawaii, United States
Hawaii Cataract Laser Institute - Maui
Kahului, Hawaii, United States
Hawaii Cataract Laser Institute - Kona
Kailua-Kona, Hawaii, United States
Countries
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Other Identifiers
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RIH 1009
Identifier Type: -
Identifier Source: org_study_id
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