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An Early Feasibility Study of a Robotically Implanted Brain-Computer Interface for Neural Control of External Devices in Spinal Cord Injury, Amyotrophic Lateral Sclerosis, and Chronic Ischemic Stroke

An Early Feasibility Study of a Robotically Implanted Brain-Computer Interface for Neural Control of External Devices in Spinal Cord Injury, Amyotrophic Lateral Sclerosis, and Chronic Ischemic Stroke

Recruiting
18 years and older
All
Phase N/A

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Overview

The purpose of this study is to evaluate the safety and preliminary effectiveness of the N1 System, a fully implanted brain-computer interface placed in the motor cortex with the R1 Robot. The study builds on knowledge gained in a previous clinical investigation of this system. It enrolls adults with severe upper-limb impairment from spinal cord injury, amyotrophic lateral sclerosis (ALS), or chronic ischemic stroke. Participants use neural signals recorded by the N1 Implant to control a computer cursor or virtual keyboard. The study will describe serious adverse device effects and will assess digital daily activities, computer-control performance, independent use of the system, and participant-, clinician-, and caregiver-reported outcomes. Up to 10 participants will be enrolled at up to five sites in the United States and followed for about 2 years after implantation, or about 3 years if they choose extended follow-up. There is no comparison group; each participant's results are compared with their own baseline.

Eligibility

Inclusion Criteria:

Adults with a diagnosis of ALS, spinal cord injury or chronic ischemic stroke who have severe weakness in the arms and hands that limits independent use of a computer or phone.

  • Stable medical, physical and psychological condition
  • Ability to communicate verbally or with a communication aid
  • A caregiver available when daily support is needed

Exclusion Criteria:

  • Morbid obesity (Body Mass Index \> 40)
  • History of poorly controlled seizures or epilepsy
  • Requires magnetic resonance imaging (MRI) for any ongoing medical conditions
  • Prior brain implant or active implanted medical device
  • Psychiatric disorder or cognitive impairment
  • Recent heart attack or cardiac arrest
  • Blood thinners that cannot be paused for surgery
  • Brain MRI or CT demonstrating hemorrhage, tumor, or distorted or adverse anatomy
  • Any condition which, in the opinion of the Investigator, would compromise your ability to safely participate in the study or undergo the implantation procedure

Study details
    Spinal Cord Injury
    Amyotrophic Lateral Sclerosis
    Chronic Ischemic Stroke
    Tetraplegia/Tetraparesis

NCT07929792

Neuralink Corp

14 November 2026

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FAQs

Learn more about clinical trials

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A clinical trial is a study designed to test specific interventions or treatments' effectiveness and safety, paving the way for new, innovative healthcare solutions.

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