Argus® II Retinal Prosthesis System Post-Market Surveillance Study
NCT01490827 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 52
Last updated 2020-05-21
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.
Conditions
- Outer Retinal Degeneration
- Retinitis Pigmentosa
Sponsors & Collaborators
-
Second Sight Medical Products
lead INDUSTRY
Principal Investigators
-
Anne-Marie Ripley · Second Sight Medical Products
Eligibility
- Min Age
- 25 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2011-11-30
- Primary Completion
- 2020-03-31
- Completion
- 2020-03-31
Countries
- Germany
- Italy
Study Locations
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