Pasadena, CANCT01958086Now 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

The investigators objective is to run human clinical trials in which brain activity recorded through a "brain-chip" implanted in the human brain can be used to provide novel communication capabilities to severely paralyzed individuals by allowing direct brain-control of a computer interface. A prospective, longitudinal, single-arm early feasibility study will be used to examine the safety and effectiveness of using a neural communication system to control a simple computer interface and a tablet computer. Initial brain control training will occur in simplified computer environments, however, the ultimate objective of the clinical trial is to allow the human patient autonomous control over the Google Android tablet operating system. Tablet computers offer a balance of ease of use and functionality that should facilitate fusion with the BMI. The tablet interface could potentially allow the patient population to make a phone call, manage personal finances, watch movies, paint pictures, play videogames, program applications, and interact with a variety of "smart" devices such as televisions, kitchen appliances, and perhaps in time, devices such as robotic limbs and smart cars. Brain control of tablet computers has the potential to greatly improve the quality of life of severely paralyzed individuals. Five subjects will be enrolled, each implanted with the NCS for a period of at least 53 weeks and up to 313 weeks. The study is expected to take at least one year and up to six years in total.

Sponsor: Richard A. Andersen, PhD

Who Can Participate

Inclusion Criteria

Pathology resulting in paralysis
Age 22-65 years
Able to provide informed consent
Understand and comply with instructions, if necessary, with the aid of a translator
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
Stable ventilator status

Exclusion Criteria

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
Medically uncontrolled diabetes
Autonomic dysreflexia
History of seizure
Implanted hydrocephalus shunt
History of supratentorial brain injury or neurosurgery
Medical conditions contraindicating surgery and chronic implantation of a medical device
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.

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 (NCT01958086) 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 (NCT01958086) 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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