Epidural Stimulation After Neurologic Damage

Part of paid clinical trials in Minneapolis, Minnesota.

Sponsor
University of Minnesota
Study ID
NCT03026816
Status
Recruiting
Apply to this trial

Conditions

  • Paraplegia, Complete
  • Spinal Cord Injuries

Eligibility Criteria

Sex
ALL
Age
22 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Epidural Spinal Cord Stimulation — DEVICE
    epidural spinal cord stimulator

Study Details

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.

Key Dates

Start date
Aug 7, 2017
Status verified
Apr 2026
Primary completion
Jan 31, 2027
Completion
Jan 31, 2028

Study Design

Enrollment
100 participants (estimated)
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT

Arms

  • Experimental: Epidural Spinal Cord Stimulation
    Epidural Spinal Cord Stimulation

Primary Outcome Measure

Change in Volitional Response Index Magnitude [ Time Frame: Months: 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15 ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
Hennepin County Medical CenterMinneapolisMinnesota55415
David Darrow, MD MPH
[email protected]
612-217-4290
Study Coordinator
[email protected]
612-873-9113
David Darrow, MD MPH (PRINCIPAL_INVESTIGATOR)

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By research site
Hennepin County Medical Center· Minneapolis, MN

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