Providing Brain Control of Extracorporeal Devices to Patients With Quadriplegia



Status:Completed
Conditions:Hospital, Neurology
Therapuetic Areas:Neurology, Other
Healthy:No
Age Range:18 - 65
Updated:1/23/2019
Start Date:February 2013
End Date:January 2019

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A Feasibility Study of the Ability of the Neural Prosthetic System to Provide Direct Brain Control of Extracorporeal Devices in Patients With Quadriplegia Due to High Spinal Cord Injury

This research study is being done to develop a brain controlled medical device, called a
brain-machine interface or BMI, that will provide people with a spinal cord injury some
ability to control an external device such as a computer cursor or robotic limb by using
their thoughts.

Developing a brain-machine interface (BMI) is very difficult and currently only limited
technology exists in this area of neuroscience. The device in this study involves implanting
very fine recording electrodes into areas of the brain that are known to create arm movement
plans and provide hand grasping information. These movement and grasp plans would then
normally be sent to other regions of the brain to execute the actual movements. By tying into
those pathways and sending the movement plan signals to a computer instead, the investigators
can translate the movement plans into actual movements by a computer cursor or robotic limb.

The device being used in this study is called the NeuroPort Array and is surgically implanted
in the brain. This device and the implantation procedure are experimental which means that it
has not been approved by the Food and Drug Administration (FDA). One NeuroPort Array consists
of a small grid of electrodes that will be implanted in brain tissue with a small cable that
runs from the electrode grid to a small hourglass-shaped pedestal. This pedestal is designed
to be attached to the skull and protrude though the scalp to allow for connection with the
computer equipment.

The investigators hope to learn how safe and effective the NeuroPort Array is in controlling
computer generated images and real world objects, such as a robotic arm, using imagined
movements of the arms and hands. To accomplish this goal, two NeuroPort Arrays will be used.


Inclusion Criteria:

- High cervical spinal lesion

- Able to provide informed consent

- Able to understand and comply with instructions in English

- Able to communicate via speech

- Surgical clearance

- Life expectancy greater than 12 months

- Live within 60 miles of study location and willing to travel up to 5 days per week

- A regular caregiver to monitor the surgical site

- Psychosocial support system

Exclusion Criteria:

- Presence of memory problems

- intellectual impairment

- Psychotic illness or chronic psychiatric disorder, including major depression

- Poor visual acuity

- Pregnancy

- Active infection or unexplained fever

- scalp lesions or skin breakdown

- HIV or AIDS infection

- Active cancer or chemotherapy

- Diabetes

- Autonomic dysreflexia

- History of seizure

- Implanted hydrocephalus shunt

- Previous neurosurgical history affecting parietal lobe function

- Medical conditions contraindicating surgery and chronic implantation of a medical
device

- Prior cranioplasty

- Unable to undergo MRI or anticipated need for MRI during study

- Nursing an infant or unwilling to bottle-feed infant

- Chronic oral or intravenous use of steroids or immunosuppressive therapy

- Suicidal ideation

- Drug or alcohol dependence

- Planning to become pregnant, or unwilling to use adequate birth control
We found this trial at
3
sites
Los Angeles, California 90033
213) 740-2311
University of Southern California The University of Southern California is one of the world’s leading...
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