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Transcutaneous and Epidural Spinal Stimulation for Enabling Motor Function in Humans With Motor Complete Paraplegia

NCT03945331 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 2

Last updated 2020-10-19

No results posted yet for this study

Summary

The purpose of this study is to compare transcutaneous electrical spinal stimulation (TESS) and epidural electrical stimulation (EES); in particular, the motor activity enabled by each method and the potential health benefits of each method.

Conditions

  • Paraplegia, Spinal
  • Paraplegia, Complete
  • Paraplegia; Traumatic

Interventions

DEVICE

Transcutaneous spinal cord stimulator

DS8R Electrical Stimulator For Human Research

DEVICE

Epidural spinal cord stimulation system

Spectra WaveWriter Epidural Spinal Cord Stimulator System with CoverEdge 32 Electrode Surgical Lead

Sponsors & Collaborators

  • Minnesota Office of Higher Education

    collaborator OTHER_GOV

  • Mayo Clinic

    lead OTHER

Principal Investigators

  • Kristin D. Zhao, Ph.D. · Mayo Clinic

Study Design

Allocation
NON_RANDOMIZED
Purpose
DEVICE_FEASIBILITY
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
22 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-01-22
Primary Completion
2020-06-17
Completion
2020-06-17
FDA Device
Yes

Countries

  • United States

Study Locations

More Related Trials

Entities

Companies

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 NCT03945331 on ClinicalTrials.gov