nVNS, CBD, and SoC for Persistent Post-Traumatic Headache

Part of paid clinical trials in Scottsdale, Arizona.

Sponsor
American Society of Pain and Neuroscience, Inc.
Study ID
NCT07624279
Phase
PHASE2
Status
Not Yet Recruiting

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Conditions

  • Persistent Post Traumatic Headache

Eligibility Criteria

Sex
ALL
Age
18 Years - 75 Years
Healthy Volunteers
Not accepted

Interventions

  • Non-Invasive Vagus Nerve Stimulation — DEVICE
    Two treatments to the cervical vagus nerve twice daily
  • Cannabidiol — DRUG
    Dosage titrated as per schedule
  • Standard of Care — DRUG
    Oral pharmacotherapy as selected by site investigator and participant

Study Details

Do cannabidiol (CBD) or vagus nerve stimulation reduce the frequency of persistent post-traumatic headache more than traditional oral headache medications?

Key Dates

Start date
Jun 1, 2026
Status verified
May 2026
Primary completion
Jul 31, 2027
Completion
Jul 1, 2028

Study Design

Enrollment
80 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT

Arms

  • Experimental: Non-Invasive Vagus Nerve Stimulation
  • Experimental: Cannabidiol
  • Experimental: Standard of Care

Primary Outcome Measure

Moderate-severe headache days [ Time Frame: Weeks 9-12 ]

Central Contacts

Locations (8)

FacilityCityStateZIP
Mayo ClinicScottsdaleArizona85054
Kerlan-Jobe Orthopaedic InstituteLos AngelesCalifornia90045
International Spine, Pain & Performance CenterWashington D.C.District of Columbia20006
Florida Spine & Pain SpecialistsTampaFlorida33614
University of Kansas Medical CenterKansas CityKansas66160
Premier Pain CenterShrewsburyNew Jersey07702
University Hospitals Cleveland Medical CenterClevelandOhio44106
Allegheny General HospitalPittsburghPennsylvania15212

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