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A Study to Evaluate the BrainPort Vision Device in Individuals Blinded by Traumatic Injury

Blindness Clinical Trial

Official title:
Safety and Efficacy of the BrainPort V200 Device in Individuals Blinded by Traumatic Injury

Clinical Trial Summary

The BrainPort V200 Device is a wearable, non-surgical, prosthetic device intended for people who are profoundly blind. The BrainPort V200 translates images captured by a digital camera into electro-tactile stimulation presented on the user's tongue to perceive shape, size, location, and motion of objects within the environment. The purpose of this study is to evaluate the safety and functional performance of the BrainPort V200 device in individuals who have been medically documented as blind, light perception or worse, due to a traumatic injury (cortical or ocular).

Clinical Trial Description

n/a

Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Supportive Care

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02393118
Study type Interventional
Source Wicab
Contact
Status Active, not recruiting
Phase N/A
Start date September 2014
Completion date September 2016
View Details
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