Microelectrode Brain-Machine Interface for Individuals With Tetraplegia

NCT01364480 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 1

Last updated 2024-01-09

Study results available
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Summary

The purpose of this research study is to demonstrate the safety and efficacy of using two NeuroPort Arrays (electrodes) for long-term recording of brain activity.

Conditions

  • Tetraplegia
  • Spinal Cord Injury

Interventions

DEVICE

Implantation of NeuroPort Arrays in the motor cortex

Two Blackrock Microsystems NeuroPort Arrays will be implanted in the motor cortex of study participants.

Sponsors & Collaborators

  • Michael Boninger

    lead OTHER

Principal Investigators

  • Michael L Boninger, MD · University of Pittsburgh

Study Design

Allocation
NA
Purpose
OTHER
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
70 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-05-01
Primary Completion
2022-11-26
Completion
2022-11-26

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01364480 on ClinicalTrials.gov