Argus II Retinal Prosthesis System Dry AMD Feasibility Study Protocol

Status Completed

Clinical Trial Summary

The purpose of this study is to test the Argus II Retinal Prosthesis System in patients with severe age-related macular degeneration (AMD). The Argus II System has already been studied in completely blind patients with retinitis pigmentosa (RP). In RP patients, some cells of the retina are irrevocably damaged and the Argus II System has been found to restore some basic visual function. On these grounds, the device has received authorization for use on the European market (the CE certification) in 2011.

Clinical Trial Description

In this study, 5 subjects with severe dry AMD who are legally blind will be implanted with the Argus II System. The study will evaluate the safety of the device and surgery, as well as functioning of the system and the extent of any restored vision. Each subject will be followed for 3 years, with their eye health and visual function tested at multiple time points. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT02227498
Study type	Interventional
Source	Second Sight Medical Products
Contact
Status	Completed
Phase	N/A
Start date	June 2015
Completion date	March 2020

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