Vagus Nerve Stimulation for Myelopathy
Part of paid clinical trials in St Louis, Missouri.
- Sponsor
- Washington University School of Medicine
- Study ID
- NCT07660250
- Status
- Recruiting
Conditions
- Degenerative Cervical Myelopathy
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Accepted
Interventions
- Vagus nerve stimulation (taVNS) — DEVICEVagus nerve stimulation - clip is attached to ear
- Sham Stimulation — DEVICEClip will be attached to the ear, but no stimulation will be given.
Study Details
The objective of this study is to generate preliminary data to establish the feasibility and effectiveness of transauricular vagus nerve stimulation (taVNS) to improve post-operative outcomes of moderate to severe degenerative cervical myelopathy (DCM)
Key Dates
- Start date
- Apr 14, 2026
- Status verified
- Jun 2026
- Primary completion
- Apr 30, 2028
- Completion
- May 31, 2028
Study Design
- Enrollment
- 36 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: Pre-Post Group (P-P)This group will undergo taVNS for up to 6 weeks before and for 3 months following surgery
- Experimental: Post GroupThis group will undergo sham stimulation for up to 6 weeks before surgery. They will receive taVNS for 3 months after surgery
- Sham Comparator: Sham GroupThis group will undergo sham stimulation for up to 6 weeks before surgery and for 3 months after surgery. The patients will not know they are not receiving stimulation.
Primary Outcome Measure
mJOA - Modified Japanese Orthopedics Association [ Time Frame: through study completion, an average of 1 year ]
Central Contacts
- Linda Koester, BS314-362-7368
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Washington University | St Louis | Missouri | 63110 | Wilson Z Ray, MD Wilson Z. Ray, MD (PRINCIPAL_INVESTIGATOR) |
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