Condition: Spinal Cord Stimulation · Electric Stimulation Therapy · Traumatic Spinal Cord Injury · Sponsor: Francis Farhadi
The study will be a non-randomized, non-blinded pilot study to analyze the safety and feasibility of a non-significant risk device, transcutaneous spinal cord stimulation. The aim is to include 30 total patients, 10 patients in each of 3 groups: 1. Non-traumatic spinal cord injury (ntSCI) with diagnosis of degenerative cervical myelopathy and offered surgical intervention. 2. Early tSCI screened during the hospital admission when cervical/thoracic spinal injury was diagnosed. 3. Delayed tSCI (control) screened 6-24 months after acute cervical/thoracic spinal injury.
This description comes directly from the study's public registry record.
H. Francis Farhadi, MD, PhD · 859-323-5661 · francis.farhadi@uky.edu
Kris P Dyer, MPH, BS · 859-323-4533 · kris.dyer@uky.edu
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| University of Kentucky - Chandler Medical Center | Lexington, Kentucky, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06520020