Investigation on the Bidirectional Cortical Neuroprosthetic System

Recruiting N/A Interventional Study
Tetraplegia Quadriplegia
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
22 – 65
Sex
Any
Study type
Interventional
Purpose
Device Feasibility
Participants needed
5 (estimated)
Sponsor
Johns Hopkins University · Other
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About This Trial

The Bidirectional Cortical Neuroprosthetic System (BiCNS) consists of NeuroPort Microelectrode Array Systems and NeuroPort Electrodes (Sputtered Iridium Oxide Film), Patient Pedestals, the NeuroPort BioPotential Signal Processing System, and the CereStim C96 Programmable Stimulator. The goals of this early feasibility study consist of safety and efficacy evaluations of this device.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: Participants must meet all inclusion criteria, verified by medical evaluation, psychological evaluation, and review of medical history. Inclusion criteria include: * Participants with C4-C6 tetraplegia from any etiology except neurodegenerative disease (e.g. amyotrophic lateral…
Contacts

Nathan E Crone, MD

4109559441

ncrone@jhmi.edu

CONTACT

Francesco Tenore, PhD

4437789774

francesco.tenore@jhuapl.edu

CONTACT