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Clinical Trial Summary

The purpose of the study is to evaluate the effectiveness and safety of the BrainPort® Vision Pro, an electronic oral assistive device, in the performance of daily tasks by French persons who have residual vision limited to light perception or less in both eyes.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04725760
Study type Interventional
Source Wicab
Contact Patricia Grant, Ph.D.
Phone 312-447-3234
Email pgrant@wicab.com
Status Recruiting
Phase N/A
Start date October 1, 2020
Completion date September 30, 2022

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