The purpose of this clinical study is to allow the investigation of the Neural Bridging System for participants with tetraplegia to assess if the investigational device can reanimate a paralyzed limb under voluntary control by the participant's thoughts.
This study plans to enroll participants who have been diagnosed with C4- C6 ASIA A spinal cord injuries (motor and sensory complete neurologic injuries), who are more than 1 year post injury, and who are neurologically stable.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
OTHER
Masking
NONE
Enrollment
1
Implanted device
The Ohio State University Wexner Medical Center - Center for Neuromodulation
Columbus, Ohio, United States
Number of Participants With Voluntary Movement
The primary outcome measure of this study is the achievement of voluntary hand movement using the neural bridge system
Time frame: 9 months
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