Bupivacaine for Post-Traumatic Headache
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial tests a treatment for headaches that occur after a head injury, using a medication called bupivacaine. Researchers aim to determine if different strengths of this medication, delivered through a simple procedure called a nerve block (specifically, a bilateral greater occipital nerve block), can reduce the frequency of these headaches. Participants will receive one of three different doses of bupivacaine or a placebo (inactive treatment). Veterans who have experienced headaches at least twice a week for three months following a head injury, with no other identified cause, may be suitable candidates. As a Phase 2 trial, this research focuses on measuring the treatment's effectiveness in an initial, smaller group of people.
Is there any evidence suggesting that this trial's treatments are likely to be safe?
Research shows that bupivacaine is usually well-tolerated for nerve blocks. This local anesthetic has been used for other types of pain relief. In past studies, patients who received bupivacaine for nerve blocks reported few serious side effects. Most often, mild reactions such as temporary numbness, dizziness, or mild soreness at the injection site occur.
Specific data on side effects for bupivacaine in greater occipital nerve blocks is not available. However, the trial aims to test the treatment's effectiveness and safety, indicating that earlier studies have found it reasonably safe.
Participants in this trial will receive different doses: 0.05% and 0.5%. These variations help determine how well each dose is tolerated. Bupivacaine already has FDA approval for other uses, supporting its general safety.
Why do researchers think this study treatment might be promising for post-traumatic headache?
Most treatments for post-traumatic headaches typically involve oral medications like NSAIDs, triptans, or muscle relaxants. But the use of bupivacaine for this condition is unique because it involves a nerve block technique, specifically targeting the greater occipital nerves. This local anesthetic approach can directly reduce headache pain by numbing the nerves involved, potentially offering faster relief than oral medications. Researchers are excited as this method could minimize systemic side effects and provide a non-opioid alternative, addressing pain at the source with precision.
What evidence suggests that bupivacaine bilateral greater occipital nerve block might be an effective treatment for post-traumatic headache?
This trial will compare different doses of bupivacaine for blocking the greater occipital nerve to reduce headache pain. Studies have shown that using bupivacaine in this manner can effectively alleviate headache pain, with effects lasting several weeks. Specifically, patients have reported improvements in headache severity for up to six months after receiving these anesthetic injections. Additionally, researchers have found nerve blocks to be very effective for managing headaches caused by trauma. Overall, these findings suggest that bupivacaine nerve block could be a promising option for people suffering from post-traumatic headaches.12345
Who Is on the Research Team?
Emmanuelle Schindler, MD, PhD
Principal Investigator
VA Connecticut Healthcare System
Are You a Good Fit for This Trial?
This trial is for veterans who have headaches after a concussion or head injury. Participants should be adults with ongoing post-traumatic headaches and able to keep a headache diary.Inclusion Criteria
Exclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Treatment
Veterans receive 0.0%, 0.05%, or 0.5% bupivacaine in bilateral GON blocks
Follow-up
Participants maintain a headache diary to measure change in headache frequency
Long-term follow-up
Participants are monitored for changes in headache-related outcomes
What Are the Treatments Tested in This Trial?
Interventions
- Bupivacaine bilateral greater occipital nerve block
Trial Overview
The study tests whether injecting different strengths of the numbing medicine bupivacaine into both sides of the back of the head (greater occipital nerve block) can reduce headache frequency. Participants are randomly assigned to one of three dose groups.
How Is the Trial Designed?
3
Treatment groups
Experimental Treatment
Active Control
Placebo Group
0.5% bupivacaine
0.05% bupivacaine
0.0% bupivacaine (normal saline)
Find a Clinic Near You
Who Is Running the Clinical Trial?
Yale University
Lead Sponsor
VA Connecticut Healthcare System
Collaborator
National Headache Foundation
Collaborator
Citations
Nerve blocks for occipital headaches: A systematic review and ...
Patient headache pain severity is improved for at least 6 months after anesthetic and corticosteroid injection, and patient headache frequency is improved for ...
Nerve Blocks in the Treatment of Headache - Neurotherapeutics
The procedure can result in rapid relief of pain and allodynia, and effects may last for several weeks.
Efficacy of Nerve Blocks for Managing Refractory ...
Conclusion: This retrospective review offers preliminary but compelling evidence that nerve blocks are a highly effective option for patients with posttraumatic ...
Greater Occipital Nerve Blockade in Veterans With Post- ...
Acute and subacute sensations from bupivacaine GON blockade will be measured and the lowest concentration that resembles the sensations elicited by full dose ( ...
5.
providerpublic.mybcbswny.com
providerpublic.mybcbswny.com/medpolicies/wellpoint/active/mp_pw_c191511.htmlSURG.00144 Occipital and Sphenopalatine Ganglion ...
The primary outcome measure was defined as a 50% or greater reduction in the frequency of days with moderate or severe migraine headache in the ...
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