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Clinical Trial Summary

In this study, the principle functionality of the device will be tested in humans for the first time. The study will evaluate the extent to which patients with atrophic dry age related macular degeneration (AMD) have evoked light perception using the implant.


Clinical Trial Description

In this study subjects are provided with a PRIMA sub-retinal implant in one eye. A camera integrated in the external components of the implant captures visual information of the environment, this information is processed by a pocket processor and then transmitted via projected IR light onto the implant. The implant received the projected IR light and stimulates the nerve cells of the retina. Interim analysis will be performed at 6 months after implantation. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03333954
Study type Interventional
Source Pixium Vision SA
Contact
Status Active, not recruiting
Phase N/A
Start date November 6, 2017
Completion date August 27, 2024

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