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RecruitingSCI - Spinal Cord Injury

Epidural Stimulation After Neurologic Damage: Long-Term Outcomes

Eligible age

22+ yrs

Accepts

All genders

Locations

1 state

Healthy volunteers

No

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About this study

This study will evaluate the long-term effect of chronic spinal cord stimulation to restore volitional movement for patients with chronic spinal cord injuries.

Sponsor: University of Minnesota

You may qualify if…

  • 22 years of age or older
  • Able to undergo the informed consent process
  • Stable spinal cord injury
  • International Standards for Neurological Classification of Spinal Cord Injury (ISNCSCI) neurologic level of injury below C5
  • No ventilator dependency within the last year
  • American Spinal Injury Association (AISA) imparement scale"A" or "B" in the absence of spinal cord stimulation
  • Medically stable in the judgment of the Principal investigator
  • Greater than 1 year since initial injury and at least 6 months from any required spinal instrumentation and 2 months from spinal cord stimulator surgery

You may not qualify if…

  • Current and anticipated need for opioid pain medications or pain that would prevent full participation in the rehabilitation program in the judgment of the principal investigator
  • Use of botulinum toxin (Botox) injections in the previous six months
  • Clinically significant mental illness in the judgment of the principal investigator
  • Other conditions or medications that would make the subject unable to participate in testing/rehabilitation in the judgment of the principal investigator
  • Nonfunctional spinal cord stimulator or near end-of-life, determined by the PI
  • Current Pregnancy
  • Current pain relief from the spinal cord stimulator if the indication for implantation was for management of chronic pain.

Where it's recruiting

Minnesota

Minneapolis

Source: ClinicalTrials.gov · NCT05705453 · last updated 2026-04-08

Epidural Stimulation After Neurologic Damage: Long-Term Outcomes · TrialPath