ECoG BMI for Motor and Speech Control

This study is testing a device called the PMT/Blackrock Combination Device. This device uses electrodes placed directly on the surface of the brain (electrocorticography or ECoG) to record brain activity. Researchers want to see if these brain signals can help people with severe neurological conditions control complex robotic systems and produce speech. You might be able to join if you are over 21 and have limited use of your upper limbs due to conditions like ALS, spinal cord injury, stroke, multiple sclerosis, or muscular dystrophies. The study will look at how safe the device is and how well it works over a period of up to six years after it's implanted. The current status of this study is unclear.

Study design
This interventional study plans to enroll 3 participants. It is not specified if it is randomized or blinded.
What's involved
Participants will have electrodes implanted on their brain and will undergo training and assessment to control a robotic system and produce speech.
Compensation
Not stated in the trial record.
Follow-up
Participants will be followed for up to 6 years after the device is 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.

NCT03698149

ECoG BMI for Motor and Speech Control

Recruiting
NAAges 21+InterventionalDevice feasibility
Karunesh Ganguly
~3 participants
Updated 2026-05-05 on ClinicalTrials.gov
What's tested:PMT/Blackrock Combination Device

At a glance

Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Incidence of Treatment-Emergent Adverse Events [Safety and Tolerability]
Measured over Up to 6 years post-implant period
+2 more outcomes measured
ALS
SCI - Spinal Cord Injury
Stroke
Multiple Sclerosis
Muscular Dystrophies
1 sites across 1 states
California1
  • Karunesh Ganguly, MD, PhD · PRINCIPAL_INVESTIGATOR · University of California, San Francisco

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  • Incidence of Treatment-Emergent Adverse Events [Safety and Tolerability]Up to 6 years post-implant period

    The primary endpoint of this study is to determine the incidence of treatment-emergent adverse events associated with the ECoG-based interface

  • NIDCD Primary Objective 1Up to 6 years post-implant period

    To enable communication via text decoded from neural signals.

  • NIDCD Primary Objective 2Up to 6 years post-implant period

    To enable communication via synthesized speech decoded from neural signals.