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Home Vision Monitoring Using the ForeseeHome Device Following Treatment of Neovascular Age Related Macular Degeneration — CNV  

Age Related Macular Degeneration Clinical Trial

Official title:
Home Vision Monitoring Using the ForeseeHome Device Following Treatment of Neovascular AMD

Clinical Trial Summary

ForeseeHome, an FDA-approved home device, was specifically designed for unsupervised Preferential-Hyperacuity-Perimeter (PHP) testing of Age Related Macular Degeneration (AMD) patients at home by characterizing central and paracentral metamorphopsia . The purpose of the current study is to evaluate if, in post-treatment patients, PHP parameters as measured with the ForeseeHome are in agreement with clinical decisions and retinal characteristics as measured with optical coherence tomography (OCT).

Clinical Trial Description

n/a

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01334294
Study type Observational
Source Notal Vision Ltd
Contact
Status Completed
Phase N/A
Start date April 2011
Completion date March 2014
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