Bupivacaine for Benign Headache in the ED
Information source: Carolinas Healthcare System
ClinicalTrials.gov processed this data on August 23, 2015 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Benign Headache
Intervention: 0.5% bupivacaine (Drug); Standard Care (Drug)
Phase: Phase 2
Status: Recruiting
Sponsored by: Sean Fox Official(s) and/or principal investigator(s): Sean Fox, MD, Principal Investigator, Affiliation: Carolinas Medical Center Greg Zahn, MD, Principal Investigator, Affiliation: Carolinas Medical Center Carey Nichols, MD, Principal Investigator, Affiliation: Carolinas Medical Center
Overall contact: Melanie M Hogg, Phone: 704-355-4288, Email: mhogg@carolinas.org
Summary
Headache is a common chief complaint of patients presenting to the emergency department
(ED), accounting for approximately 3 million ED visits per year. Headache treatment is often
a source of frustration for both patients and providers. By the time patients with benign
headaches arrive in the emergency department, they have often failed non-invasive
therapeutic attempts and providers are often left with few therapeutic options. Treatment of
benign headache varies between providers, often including systemic medications with a
multitude of possible side effects. In recent years, there has been preliminary
investigation into anesthetic injections for the undifferentiated headache patient
presenting to the emergency department. It has been proposed that these patients presenting
with benign headache might benefit from this novel treatment.
Patients that present to the Emergency Department with a diagnosis of benign or primary
headache with serious or life-threatening causes of headache will be offered enrollment into
the study.
Following consent, subjects will receive either 0. 5% bupivacaine injected bilaterally in the
paraspinal musculature of the cervical spine or the standard treatment with intravenous
Prochlorperazine. The subjects will complete a validated pain scale before, and 20 minutes
after injection. At twenty minutes post-injection, the subject will be reevaluated for
symptoms. The subject will then be eligible for discharge or standard treatment at the
discretion of the treating physician.
Subjects will be followed for 72 hours after enrollment for headache recurrence. Subjects
will be monitored for immediate and post-discharge complications.
Clinical Details
Official title: Treatment of Benign Headache in the Emergency Department Population With Lower Cervical Paraspinous Bupivacaine Injections Versus Anti-Emetic Treatment in the Emergency Department Population: Randomized Prospective Control Trial
Study design: Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
Primary outcome: Length of stayIncidence of immediate and post-discharge complications.
Secondary outcome: Symptomatic relief of headache
Detailed description:
Headache is a common chief complaint of patients presenting to the emergency department
(ED), accounting for approximately 3 million ED visits per year. Headache treatment is often
a source of frustration for both patients and providers. By the time patients with benign
headaches arrive in the emergency department, they have often failed non-invasive
therapeutic attempts and providers are often left with few therapeutic options. Treatment of
benign headache varies between providers, often including systemic medications with a
multitude of possible side effects. Additionally, most headache cocktails require prolonged
duration of treatment, occupying valuable bed space in increasingly busy emergency
departments.
In recent years, there has been preliminary investigation into anesthetic injections for the
undifferentiated headache patient presenting to the emergency department. It has been
proposed that these patients presenting with benign headache might benefit from this novel
treatment. Since 2003, paraspinal muscle injections of bupivacaine have been used in
emergency department patients with encouraging results. The mechanism of action is not
clearly understood; however, it has been proposed that these injections affect the
trigeminocervical complex hypothesized to play an integral role in headache physiology,
similar to the same mechanism behind greater occipital nerve blocks used by neurologists.
To the best of the investigators knowledge, there has never been a prospective
double-blinded randomized control trial addressing this novel approach to headache
management. Even so, the topic of using bupivacaine to inject the paraspinal musculature of
the cervical spine has gained wider recognition over the past year. The topic has been
discussed heavily on emergency medicine blogs and podcasts. Additionally, online videos have
been posted to educate emergency medicine providers on the injection technique. According to
retrospective literature, clinical efficacy was observed with a significant proportion of
the patients receiving therapeutic effect. These studies, along with anecdotal experience
with the procedure at the investigators institution, have led to great excitement concerning
the possibility of a new approach to emergency department headache management. However, the
topic still needs investigation with a well-designed prospective clinical trial to determine
true clinical utility.
Eligibility
Minimum age: 18 Years.
Maximum age: 65 Years.
Gender(s): Both.
Criteria:
Inclusion Criteria:
1. Age 18-65 years old
2. Diagnosis of benign or primary headache
Exclusion Criteria:
1. Hypersensitivity or allergy to bupivacaine (amide anesthetics) or prochlorperazine or
other drugs in the same class, dopaminergic blockers.
2. Overlying signs of infection at site of injection (Erythema, purulence, open skin)
3. Neck pathology ( History of surgery to the cervical spine, History of surgical
hardware in place, Documented disc abnormality, History of vertebral artery or
carotid artery dissection, Torticollis)
4. Intracranial abnormality/pathology (Tumor, Hemorrhage, Concussion or post concussive
syndrome)
5. History of increased intracranial pressure (ICP)
6. A known history of extrapyramidal symptoms, dystonia, parkinsonism, tardive
dyskinesia or neuroleptic malignant syndrome
7. Known pregnancy
8. Narcotic seeking patients as determined by the treating physician with optional
assistance from medical record review and North Carolina Drug Database
Locations and Contacts
Melanie M Hogg, Phone: 704-355-4288, Email: mhogg@carolinas.org
Carolinas Medical Center, Charlotte, North Carolina 28203, United States; Recruiting Melanie M Hogg, Phone: 704-355-4288, Email: mhogg@carolinas.org
Additional Information
Starting date: October 2013
Last updated: February 6, 2015
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