Purpose

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.

Condition

Eligibility

Eligible Ages
Over 18 Years
Eligible Sex
All
Accepts Healthy Volunteers
No

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.

Study Design

Phase
Phase 1/Phase 2
Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel Assignment
Primary Purpose
Treatment
Masking
Triple (Participant, Care Provider, Investigator)

Arm Groups

ArmDescriptionAssigned Intervention
Placebo Comparator
Placebo
0.0% bupivacaine (normal saline)
  • Other: Bupivacaine bilateral greater occipital nerve block
    Three subcutaneous injections of 1 mL each will be injected on both sides of the occipital region around the greater occipital nerve.
Active Comparator
Low dose bupivacaine
0.05% bupivacaine
  • Other: Bupivacaine bilateral greater occipital nerve block
    Three subcutaneous injections of 1 mL each will be injected on both sides of the occipital region around the greater occipital nerve.
Experimental
Full dose bupivacaine
0.5% bupivacaine
  • Other: Bupivacaine bilateral greater occipital nerve block
    Three subcutaneous injections of 1 mL each will be injected on both sides of the occipital region around the greater occipital nerve.

Recruiting Locations

VA Connecticut Healthcare System
West Haven, Connecticut 06516
Contact:
Emmanuelle Schindler, MD, PhD
203-932-5711
emmanuelle.schindler@va.gov

More Details

Status
Recruiting
Sponsor
Yale University

Study Contact

Emmanuelle Schindler, MD, PhD
203-932-5711
emmanuelle.schindler@va.gov

Detailed Description

Military Servicemembers are at elevated risk for traumatic brain injury (TBI) and its consequences, including post-traumatic headache (PTH). The most common phenotype of PTH is migraine, for which there are numerous potential treatments, though these have limitations, including poor efficacy, drug-drug interactions, and intolerable side effects. Therefore, the consideration of other methods to manage PTH in Servicemembers and Veterans is warranted. Anesthetic greater occipital nerve (GON) blockade is a simple, inexpensive, and safe procedure that has demonstrable headache pain suppressing effects in a variety of headache disorders. This intervention is frequently done to provide immediate relief, followed by a period of reduced headache burden. In this second portion of this study, Veterans with chronic post-traumatic headache will be randomized to receive 0.0%, 0.05%, or 0.5% bupivacaine in bilateral GON blocks. They will maintain a headache diary to measure the change in headache frequency over the two months after injection. This design uses information gathered from sub-study 1 of this project (NCT#06069791). In that initial intervention, different concentrations of bupivacaine were examined to consider the intensity and spread of acute and subacute sensations that occur with GON blockade. This allowed us to select a low dose (0.05%) that approximates the sensations of the full dose of 0.5%.

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.