RecruitingNot ApplicableNCT06701422

Targeting Cervical Epidural Spinal Cord Stimulation for Functional Recovery


Sponsor

Columbia University

Enrollment

36 participants

Start Date

Dec 6, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

The proposed study seeks to understand how the cervical spinal cord should be stimulated after injury through short-term physiology experiments that will inform a preclinical efficacy trial. The purpose of this study is to determine which cervical levels epidural electrical stimulation (EES) should target to recruit arm and hand muscles effectively and selectively in spinal cord injury (SCI).


Eligibility

Min Age: 18 Years

Inclusion Criteria1

  • •Clinical indication for cervical spine surgery.

Exclusion Criteria1

  • •Stimulation devices in the neck or chest (e.g., vagal nerve stimulation, cardiac patients with pacemakers)

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

PROCEDUREIntraoperative stimulation of the cervical spinal cord

The surgeon will place spinal cord electrodes on the epidural surface, with stimulation sites identified using preoperative MRI. Recruitment curves will be generated by systematically increasing the stimulation intensity across various parameter combinations, including frequency, pulse count, pulse shape, and electrode-specific properties such as size, separation, and arrangement.


Locations(2)

Columbia University Irving Medical Center

New York, New York, United States

The Daniel and Jane Och Spine Hospital at NewYork-Presbyterian/Allen

New York, New York, United States

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT06701422


Related Trials