Greater Occipital Nerve Blockade in Veterans With Post-concussion Headache: Sub-study 2

Part of paid clinical trials in West Haven, Connecticut.

Sponsor
Yale University
Study ID
NCT07796074
Phase
PHASE1/PHASE2
Status
Recruiting

Conditions

  • Post-Traumatic Headache

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Bupivacaine bilateral greater occipital nerve block — OTHER
    Three subcutaneous injections of 1 mL each will be injected on both sides of the occipital region around the greater occipital nerve.

Study Details

Anesthetic greater occipital nerve (GON) blockade is a simple, inexpensive, and safe procedure that has demonstrable headache pain suppressing effects. In this study, Veterans with post-traumatic headache will be randomized to receive 0.0%, 0.05%, or 0.5% bupivacaine in bilateral GON blocks and the lasting (i.e., transitional) effects on headache frequency measured in a headache diary.

Key Dates

First listed
Aug 31, 2026
Start date
Sep 1, 2026
Status verified
Aug 2026
Primary completion
Sep 30, 2027
Completion
Dec 31, 2027

Study Design

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

Arms

  • Placebo Comparator: Placebo
    0.0% bupivacaine (normal saline)
  • Active Comparator: Low dose bupivacaine
    0.05% bupivacaine
  • Experimental: Full dose bupivacaine
    0.5% bupivacaine

Primary Outcome Measure

Change in headache days/week in the first month [ Time Frame: From one month before to one month after injection ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
VA Connecticut Healthcare SystemWest HavenConnecticut06516
Emmanuelle Schindler, MD, PhD
203-932-5711

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