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Epidural Stimulation After Neurologic Damage

NCT03026816 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 100

Last updated 2026-04-08

No results posted yet for this study

Summary

This study will evaluate a method to optimize parameter settings in epidural spinal cord stimulation used to recover lower extremity volitional movement. The study will also characterize improvement in autonomic function (such as blood pressure control) and other functions related to spinal cord injury.

Conditions

  • Spinal Cord Injuries
  • Paraplegia, Complete

Interventions

DEVICE

Epidural Spinal Cord Stimulation

epidural spinal cord stimulator

Sponsors & Collaborators

  • Minnesota Office of Higher Education

    collaborator OTHER_GOV

  • Hennepin Healthcare Research Institute

    collaborator OTHER

  • Hennepin County Medical Center, Minneapolis

    collaborator OTHER

  • University of Minnesota

    lead OTHER

Principal Investigators

  • David Darrow, MD · University of Minnesota

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
22 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-08-07
Primary Completion
2027-01-31
Completion
2028-01-31
FDA Device
Yes

Countries

  • United States

Study Locations

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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 NCT03026816 on ClinicalTrials.gov