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Transcutaneous and Epidural Stimulation in SCI

NCT04627441 · Status: WITHDRAWN · Phase: NA · Type: INTERVENTIONAL

Last updated 2022-10-04

No results posted yet for this study

Summary

The study seeks to improve the scientific understanding of how two electrical stimulation techniques, one which delivers electricity to the skin surface over the spine (transcutaneous electrical spinal stimulation \[TESS\]) and another which is implanted onto the dura mater of the spinal cord (epidural electrical stimulation \[EES\]), facilitate spinal circuitry to enable function after SCI.

Conditions

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

Interventions

DEVICE

Transcutaneous spinal cord stimulator

DS8R Electrical Stimulator For Human Research

DEVICE

Epidural spinal cord stimulator system

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

Sponsors & Collaborators

  • Kristin Zhao, PhD

    lead OTHER

Principal Investigators

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

Study Design

Allocation
NA
Purpose
BASIC_SCIENCE
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
22 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-12-16
Primary Completion
2025-12-16
Completion
2025-12-16
FDA Device
Yes

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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 NCT04627441 on ClinicalTrials.gov