Study details
Enrolling now
Augmenting Rehabilitation Outcomes and Functional Neuroplasticity Using Epidural Stimulation of Cervical Spinal Cord
The Methodist Hospital Research Institute
NCT IDNCT06225245ClinicalTrials.gov data as of Apr 2026
Target enrollment
12
Study length
about 2.4 years
Ages
22–65
Locations
1 site in TX
About this study
This trial is testing whether epidural spinal stimulation can help improve rehabilitation outcomes and functional neuroplasticity in people with cervical spinal cord injuries. It uses a device called the CoverEdgeX 32 Surgical Lead system, which has been approved for pain management but is being used as an investigational treatment for spinal cord injury.
Based on ClinicalTrials.gov records.
What participants do
- 1.Use Epidural Spinal Stimulation (ESS)
Participation effort
Estimated from trial records. Details can vary by site.
Time + visits
Low13%
Logistics
Moderate50%
Logistics difficulty varies by site location and availability.
Trial highlights
Treatment details
Auto-extracted from trial records to preview treatments and outcomes.
Body systems
Neurology