A Study to Evaluate the BrainPort® Vision Device in Subjects Who Are Blind

Status Completed

Clinical Trial Summary

The purpose of this study is to assess the safety of the BrainPort vision device and to demonstrate improved object recognition and word identification and ambulation with use of the BrainPort vision device in subjects who are medically documented as blind, with acuity of 20/ 5000 or worse.

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

Blindness

Clinical Trial Details

NCT number	NCT01488786
Study type	Interventional
Source	Wicab
Contact
Status	Completed
Phase	N/A
Start date	October 2011
Completion date	April 2013

View Details

See also
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