Cortical Recording and Stimulating Array Brain-Machine Interface for Paralysis

This study is testing a new approach for people with severe paralysis due to conditions like spinal cord injury or amputation. It involves implanting two small devices called CRS Arrays (microelectrodes) into your brain. One array records brain signals related to movement, and the other sends tiny electrical pulses to create sensations. The goal is to see if these arrays are safe for long-term use and if they can help you control devices with your thoughts or feel sensations. You might be able to join if you are between 22 and 70 years old and have very limited or no use of one or both hands. The main way we'll know if the study is successful is by checking your safety for one year after the arrays are implanted. The current status of this study is unclear.

Study design
This is an interventional study planning to enroll 30 participants. It involves implanting two CRS Arrays into the brain.
What's involved
You would have two CRS Arrays implanted in your brain. Your safety will be measured for one year following this implantation.
Compensation
Not stated in the trial record.
Follow-up
Your safety will be monitored for one year after the arrays are implanted.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT01894802

Cortical Recording and Stimulating Array Brain-Machine Interface

Recruiting
NAAges 22–70Interventional
Michael Boninger
~30 participants
Updated 2026-05-20 on ClinicalTrials.gov
What's tested:Implantation of CRS Arrays

At a glance

Recruiting sites
2 of 2 listed sites are recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
The primary outcome is the safety of the participant.
Measured over One year following array implantation
Tetraplegia
Spinal Cord Injury
Brainstem Stroke
Brachial Plexus Injury
Above Elbow Amputation
2 sites across 2 states
Illinois1
Pennsylvania1
  • Michael L Boninger, MD · PRINCIPAL_INVESTIGATOR · University of Pittsburgh

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  • The primary outcome is the safety of the participant.One year following array implantation

    This measure will be considered a success if the device is not removed for safety reasons during the 12-month post-implant evaluation.