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
20 participants
OBSERVATIONAL
2008-03-31
2013-03-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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1
Subjects diagnosed as intermediate AMD
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Subjects diagnosed as intermediate AMD in at least one eye
* Age \>50 years
* VA with habitual correction \>20/60 in the study eye
* Ability to speak, read and understand instructions in Hebrew
* Familiar with computer usage
Exclusion Criteria
* Presence of any significant media opacity that precludes a clear view of the macular area as identified in the study eye by biomicroscopy, CFP.
* Any non-macular related ocular surgery performed within 3 months prior to study entry in the target eye
* Participation in another study with the exclusion of AREDS study
* Patients diagnosed with geographic atrophy (GA)
50 Years
ALL
No
Sponsors
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Notal Vision Ltd.
INDUSTRY
Responsible Party
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Principal Investigators
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Yaron Mr Lang, MD
Role: PRINCIPAL_INVESTIGATOR
Haemek Hospital
Locations
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Haemek Medical center
Afula, , Israel
Countries
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Related Links
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sponsor site
Other Identifiers
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0197-07
Identifier Type: -
Identifier Source: secondary_id
HMP-PU1
Identifier Type: -
Identifier Source: org_study_id
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