VEGF Gene Association With Response to Neovascular Age-related Macular Degeneration With Anti-VEGF Agents
NCT ID: NCT01655589
Last Updated: 2012-08-02
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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UNKNOWN
74 participants
OBSERVATIONAL
2008-01-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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CASE_ONLY
RETROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
* Visual acuity better than 20/400
* Loading dose with three intravitreal injections of anti-VEGF agents, administred one per month over three months
* Follow-up period of at least six months
Exclusion Criteria
* Eyes with polypoidal choroidal vasculopathy
* Eyes previously submitted to posterior vitrectomy
* Other diseases that could affect visual acuity
50 Years
ALL
No
Sponsors
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Institute of Vision, Brasil
OTHER
Responsible Party
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Locations
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Institute of Vision
Belo Horizonte, Minas Gerais, Brazil
Countries
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Facility Contacts
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Andre B Ferreira
Role: primary
Other Identifiers
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IV-01
Identifier Type: -
Identifier Source: org_study_id