Condition: Spinal Cord Injuries · Cervical Spinal Cord Injury · Sponsor: The Methodist Hospital Research Institute
The goal of this study is to investigate the effects of cervical epidural spinal stimulation with upper extremity training. This is an investigational study. The device used for epidural spinal stimulation (ESS) to deliver spinal stimulation is called the CoverEdgeX 32 Surgical Lead system. This device is approved by the Food and Drug Administration (FDA) for the treatment of severe pain and to manage chronic pain when other treatments have not been effective. In this study, the device is considered an investigational device because it is not approved for use in the treatment of spinal cord injury
This description comes directly from the study's public registry record.
Jenny Dinh · 346-238-4654 · jtdinh@houstonmethodist.org
Rachel Markley · 713-441-3770 · rmarkley@houstonmethodist.org
Always discuss trial participation with your own doctor first.
| The Methodist Hospital Research Institute | Houston, Texas, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06225245