Epidural Stimulation After Neurologic Damage: Long-Term Outcomes

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age22+
SponsorUniversity of Minnesota

About this trial

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

Eligibility criteria

Qualifiers

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

Disqualifiers

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

Trial design

Treatments tested in this trial

  • Epidural Spinal Cord Stimulation

Treatment groups

50 Participants
are divided into 1 treatment group

Sponsors and collaborators