About this trial

The VOICE Study is an early feasibility study to evaluate the initial clinical safety and efficacy of the N1 and R1 Systems device design concept in providing an ability to communicate. The Neuralink N1 Implant is intended to provide the ability to communicate to individuals with severe and irreversible speech production impairment. It is indicated for adults with neurological conditions of the central speech pathways who have impaired upper limb function. The N1 Implant is a skull-mounted, wireless, rechargeable implant connected to electrode threads that are implanted in the brain by the R1 Robot, a robotic electrode thread inserter.

Eligibility criteria

Qualifiers

Life expectancy ≥ 12 months.

Ability to communicate in English

Presence of a stable caregiver

Disqualifiers

Moderate to high risk for serious perioperative adverse events

Morbid obesity (Body Mass Index > 40)

History of poorly controlled seizures or epilepsy

History of poorly controlled diabetes

Trial design

Treatments tested in this trial

  • N1 Implant
  • R1 Robot

Treatment groups

6 Participants
are divided into 1 treatment group

Locations

1
The University of Texas Southwestern Medical Center75390, DallasTexas, United States

Sponsors and collaborators

Neuralink Corp

Lead sponsor