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New Enrollment Post-Approval Study of the Argus® II Retinal Prosthesis System

Retinitis Pigmentosa Clinical Trial

Official title:
New Enrollment Post-Approval Study of the Argus® II Retinal Prosthesis System

Clinical Trial Summary

This post-approval study is being implemented to monitor the use of Argus II System in a larger US population than available within pre-approval studies. An attempt will be made to include all eligible and willing subjects implanted with Argus II System in the United States.

Clinical Trial Description

Safety data will be monitored to ensure continued acceptability of risks to study subjects. The utility (i.e. visual function and functional vision) and reliability of Argus II System will also be evaluated. There is no study hypothesis. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01860092
Study type Observational
Source Second Sight Medical Products
Contact
Status Terminated
Phase
Start date January 2014
Completion date March 2020
View Details
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