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
What this study is about
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.
Simplified from trial records by PatientMatch.
What you may be asked to do
- 1.Use Epidural Spinal Stimulation (ESS)
Participation Burden
What's physically and logistically required of participants.
Logistics & Travel
In-person visits
Requires travel to a study site
Physical Intervention
Standard
How treatment is administered
Treatment Assignment
All receive treatment
Everyone gets the investigational treatment.
Extracted study details
Pulled from the trial record to show what is being tested and what the study is measuring.
Body systems
Neurology