Greater Occipital Nerve Blockade in Veterans With Post-concussion Headache: Sub-study 1
Part of paid clinical trials in West Haven, Connecticut.
- Sponsor
- Yale University
- Study ID
- NCT06069791
- Phase
- PHASE1
- Status
- Recruiting
Conditions
- Post-Traumatic Headache
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Bupivacaine Injection — DRUGsubcutaneous injection around bilateral greater occipital nerves
Study Details
The acute and subacute sensations that occur on the scalp with injection of different concentrations of bupivacaine for grater occipital nerve blockade will be compared. Each Veteran participant will be randomized to receive three different concentrations, which will be injected one week apart each.
Key Dates
- Start date
- Jan 26, 2024
- Status verified
- Jan 2026
- Primary completion
- Dec 31, 2026
- Completion
- Dec 31, 2026
Study Design
- Enrollment
- 12 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- CROSSOVER
- Primary purpose
- OTHER
Arms
- Experimental: Group 1bupivacaine 0.0%, 0.01%, and 0.05% in random order, one week apart each
- Experimental: Group 2bupivacaine 0.1%, 0.05%, and 0.1% in random order, one week apart each
- Experimental: Group 3bupivacaine 0.0%, 0.1%, and 0.5% in random order, one week apart each
- Experimental: Group 4bupivacaine \[0.01% or 0.05%\], \[0.05% or 0.1%\], and 0.05% in random order, one week apart each
Primary Outcome Measure
Acute sensation felt during injection: quality [ Time Frame: During injection ]
Central Contacts
- Emmanuelle Schindler, MD, PhD203-932-5711
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| VA Connecticut Healthcare System | West Haven | Connecticut | 06516 |
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