Pasadena, CANCT01964261Now EnrollingIRB Ready

Quadriplegia Clinical Trial in Pasadena, CA

Access cutting-edge quadriplegia treatment through this clinical trial at a research site in Pasadena. Study-provided care at no cost to qualified participants.

Sponsored by Richard A. Andersen, PhD

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Expert Care in Pasadena

Access quadriplegia specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related quadriplegia treatment provided free

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Check if you qualify for this quadriplegia clinical trial in Pasadena, CA

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Your information is protected and will only be shared with the research team.

Why Participate?

  • No-Cost Study Care

  • Local to Pasadena

    Convenient for CA residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Pasadena site if eligible
  4. 4Begin participation

About This Quadriplegia Study in Pasadena

This research study is being conducted to develop a brain controlled medical device, called a brain-machine interface. The device 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 along with sensory feedback. Development of a brain-machine interface is very difficult and currently only limited technology exists in this area of neuroscience. Other studies have shown that people with high spinal cord injury still have intact brain areas capable of planning movements and grasps, but are not able to execute the movement plans. 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 and sense feeling in the hand and fingers. 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. A key part of this study is to electrically stimulate the brain by introducing a small amount of electrical current into the electrodes in the sensory area of the brain. This will result in the sensation of touch in the hand and/or fingers. This stimulation to the brain will occur when the robotic limb touches the object, thereby allowing the brain to "feel" what the robotic arm is touching. 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 and 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 through the scalp to allow for connection with the computer equipment. The top portion of the pedestal has a protective cover that will be in place when the pedestal is not in use. The top of this pedestal and its protective cover will be visible on the outside of the head. Three Neuroport Arrays and pedestals will be implanted in this study so three of these protective covers will be visible outside of the head. It will be possible to cover these exposed portions of the device with a hat or scarf. The investigators hope to learn how safe and effective the Neuroport array plus stimulation is in controlling computer generated images and real world objects, such as a robotic arm, using imagined movements of the arms and hands.

Sponsor: Richard A. Andersen, PhD

Who Can Participate

Inclusion Criteria

High cervical spinal lesion
Able to provide informed consent
Able to understand and comply with instructions in English
Communicate via speech
Surgical clearance
Life expectancy greater than 12 months
Travel up to 60 miles to study locations up to five days per week
Caregiver monitor for surgical site complications and behavioral changes on a daily basis
Psychosocial support system

Exclusion Criteria

Presence of memory problems
Intellectual impairment
Psychotic illness or chronic psychiatric disorder, including major depression if untreated
Poor visual acuity
Active infection or unexplained fever
Scalp lesions or skin breakdown
HIV or AIDS infection
Active cancer or chemotherapy
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
Implanted Cardiac Defibrillator, Pacemaker, vagal nerve stimulator, or spinal cord stimulator.
Implanted deep brain stimulator (DBS), DBS leads, or cochlear implant.

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Pasadena?

Yes, this clinical trial (NCT01964261) has an active research site in Pasadena, CA that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Quadriplegia Treatment Options in Pasadena, CA

If you're searching for quadriplegia treatment options in Pasadena, CA, this clinical trial (NCT01964261) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Pasadena research site is actively enrolling participants for this clinical trial. You'll receive care from experienced quadriplegia specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all quadriplegia clinical trials near you to find additional studies recruiting in your area.

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