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NCT07796074
Greater Occipital Nerve Blockade in Veterans With Post-concussion Headache: Sub-study 2
Conditions: Post-Traumatic Headache
Sex: All
Ages: 18 Years – N/A
Healthy volunteers: No
Phase: PHASE2
Enrollment: 36
Sponsor: Yale University
Location: VA Connecticut Healthcare System West Haven Connecticut
Summary
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.
Eligibility Criteria
Inclusion Criteria:
* United States Military Veterans within VA Connecticut Healthcare System1.
* Head injury with headaches that have continued to occur for at least three months after the head injury
* At least two headache days per week
* Review of the medical record does not reveal another source for headache
Exclusion Criteria:
* Skull defect
* Other contraindication to bupivacaine
* Allergy or adverse reaction (e.g., rash, cardiac effects) to amide anesthetics, such as lidocaine
* Instruction from clinician to avoid amide anesthetics, such as lidocaine
* Pregnant or lack of adequate birth control
* Clinical review of the patient's case reveals red flag signs or symptoms (e.g., side-locked pain, unilateral numbness/weakness during headache, rapid ascension to peak pain, syncope during attacks) that warrant further work-up (e.g., MRI, arterial imaging).
* Absence of imaging warranted by the standard of clinical care for the head injury with headaches.
Source: ClinicalTrials.gov (NCT07796074). StuddyBuddy aggregates publicly available trial information.