Argus® II Retinal Prosthesis System Post-Market Surveillance Study

Status Terminated

Clinical Trial Summary

This post-market surveillance study is conducted in the European Economic Area where Argus II has been CE certified for use in outer retinal degeneration patients.

Clinical Trial Description

This study is being conducted to monitor the use of Argus II in a larger population than available within pre-market approval studies. Safety data will be monitored to ensure continued acceptability of risks to study participants, and an attempt will be made to include all eligible and willing participants implanted with Argus II. Measures of visual function that may contribute to device improvements will also be gathered and evaluated. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT01490827
Study type	Observational
Source	Second Sight Medical Products
Contact
Status	Terminated
Phase
Start date	November 2011
Completion date	March 31, 2020

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