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Clinical Trial Summary

The purpose of this study is to evaluate the usability of the Foresee Home device with intermediate AMD patients.


Clinical Trial Description

The AMD usability study is a prospective, longitudinal, multi-center, observational study of patients diagnosed with intermediate (dry) AMD who have been asked by their doctor to use the ForeseeHomeTM device to record the natural progression of their AMD, including conversion from the dry to wet stage. ;


Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


NCT number NCT00963339
Study type Observational
Source Notal Vision Ltd
Contact
Status Completed
Phase N/A
Start date September 2009
Completion date September 2010

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