Actively Recruiting
Visuomotor Prosthetic for Paralysis
Led by Richard A. Andersen, PhD · Updated on 2026-03-18
2
Participants Needed
3
Research Sites
930 weeks
Total Duration
On this page
Sponsors
R
Richard A. Andersen, PhD
Lead Sponsor
U
University of California, Los Angeles
Collaborating Sponsor
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Visuomotor Prosthetic for Paralysis
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Pathology resulting in paralysis
- Age 22-65 years
- Able to provide informed consent
- Understand and comply with instructions, with or without 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
- Have a regular caregiver to monitor the surgical site
- Have psychosocial support system
- Stable ventilator status
You will not qualify if you...
- Intellectual impairment
- Psychotic illness or chronic psychiatric disorder, including untreated major depression
- Poor visual acuity
- Pregnancy
- Active infection or unexplained fever
- Scalp lesions or skin breakdown
- HIV or AIDS infection
- Active cancer or undergoing chemotherapy
- Medically uncontrolled diabetes
- Autonomic dysreflexia
- History of seizure
- Implanted hydrocephalus shunt
- History of supratentorial brain injury or neurosurgery
- Medical conditions contraindicating surgery or chronic device implantation
- Unable to undergo MRI or need for MRI during study
- Nursing an infant or unwilling to bottle-feed infant
- Chronic oral or intravenous steroid or immunosuppressive therapy
- Suicidal ideation
- Drug or alcohol dependence
- Planning pregnancy or unwilling to use adequate birth control
- Implanted cardiac defibrillator, pacemaker, vagal nerve stimulator, or spinal cord stimulator
AI-Screening
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Trial Site Locations
Total: 3 locations
1
University of California Los Angeles
Los Angeles, California, United States, 90095
Actively Recruiting
2
California Institute of Technology
Pasadena, California, United States, 91125
Actively Recruiting
3
Casa Colina Centers for Rehabilitation
Pomona, California, United States, 91769
Actively Recruiting
Research Team
A
Ausaf Bari, MD, PhD
CONTACT
E
Emily Rosario, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
BASIC_SCIENCE
Number of Arms
1
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