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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WITHDRAWN
OBSERVATIONAL
2014-12-31
2015-07-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
CROSS_SECTIONAL
Study Groups
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Group 1
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* competence to understand and willingness to sign an informed consent form and participate in the study,
* pupils that dilate to 5 mm or more.
* corrected visual acuities better than 20/30,
* intraocular pressure less than 21 mm Hg,
* no family history of AMD,
* no history of ophthalmic surgery or neurologic disease,
* no history of diabetes, glaucoma, or a history of elevated intraocular pressure.
The recruitment will ensure that approximately 40 subjects will fall into each of the three age groups, 50 to 60 years, 61 to 70 years, and 71 years and older. One eye of each subject will be selected at random to be included in the study.
Exclusion Criteria
50 Years
ALL
Yes
Sponsors
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US Department of Veterans Affairs
FED
Responsible Party
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Principal Investigators
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Mahnaz Shahidi, PhD
Role: PRINCIPAL_INVESTIGATOR
Jesse Brown VA Medical Center, Chicago, IL
Locations
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Jesse Brown VA Medical Center, Chicago, IL
Chicago, Illinois, United States
Countries
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Other Identifiers
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C7002-R
Identifier Type: -
Identifier Source: org_study_id
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