Retinitis Pigmentosa Clinical Trial
Official title:
Observational Study of the Argus® II Retinal Prosthesis System
The Argus II Retinal Implant is a revolutionary new device, which offers vision to patients who are blind from retinal degeneration - retinitis pigmentosa. These patients have no alternatives. Patients typically can achieve ambulatory vision.
This study is an investigator-sponsored, observational, controlled, prospective,
single-center study. The purpose of this current study is how it affects people's visual
function and activities of daily living and to collect additional data on Argus II users in
order to monitor the System's safety. In addition, data about the long-term reliability of
the System will be gathered.
The Argus II retinal implant will be surgical implanted into patients who are blind but the
surgical procedure is not a part of this observational study. Our hypothesis is that the
visual results in our hands will be comparable to those reported in the FDA study. We will
use the results of this study to plan future enhancements to the service and to explore the
use of the device for other blinding conditions.
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Observational Model: Case-Only, Time Perspective: Prospective
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