Clinical Trials and Studies

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Study Title Principal Investigator
Argus® II Retinal Prosthesis System Post-Market Surveillance Study
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.
Active, not recruiting | Retinitis Pigmentosa | Multisite
Anne-Marie Ripley
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