Expired Study
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Minneapolis, Minnesota 55404


Purpose:

This is an open-label study assessing electrophysiologic testing of the retina with Electoretinogram (ERG) /Electrooculogram (EOG) tests in patients with exudative age-related macular degeneration (AMD). The standard FDA-approved treatment for wet AMD is ranibizumab (Lucentis). This study focuses on the ERG and EOG tests to evaluate retinal responses to ranibizumab treatment in AMD.


Criteria:

Inclusion Criteria: - Ability to provide written informed consent and comply with study assessments for the full duration of the study - Age >55 years - Patients to be included in the study must have AMD with choroidal neovascularization - BCVA between 20/20 - 20/400 - Lesion size less than or equal to 12 MPS disc areas Exclusion Criteria: - Prior treatment with an anti-VEGF agent within 6 months of enrollment in this study - Pregnancy (positive pregnancy test) - Premenopausal women not using adequate contraception. The following are considered effective means of contraception: surgical sterilization or use of oral contraceptives, barrier contraception with either a condom or diaphragm in conjunction with spermicidal gel, an IUD, or contraceptive hormone implant or patch - Prior enrollment in the study - Any other condition that the investigator believes would pose a significant hazard to the subject if the investigational therapy were initiated - Participation in another simultaneous medical investigation or trial - Media insufficient to obtain a view - Other causes of CNV not related to AMD - Active ocular or peri-ocular infection - Ocular surgery within 1 month prior to the study


NCT ID:

NCT00791427


Primary Contact:

N/A


Backup Contact:

N/A


Location Contact:

Minneapolis, Minnesota 55404
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: October 09, 2019

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