Paracervical Injection for Headache in the Emergency Department

Sponsor
Christian Fromm, MD (Other)
Overall Status
Recruiting
CT.gov ID
NCT04109885
Collaborator
(none)
108
1
2
36
3

Study Details

Study Description

Brief Summary

Headache is one of the most common presenting complaints in the emergency department.1 By the time patients with benign headaches present for treatment in the ED, they often have exhausted non-invasive treatments, and physicians are left with few therapeutic options. The investigators therefore propose to study the use of paracervical injection as a novel approach to managing headache in the emergency department. This procedure has great potential, if efficacious, to provide a safe, rapidly effective, non-sedating treatment for headache that does not involve intravenous line placement and systemic medication administration. To date, there are no published trials that evaluate this technique in this setting. The investigators intend to compare the efficacy of paracervical injection to standard first-line therapy (intravenous prochlorperazine and diphenhydramine) for the treatment of benign headache of any etiology in the emergency department.

Condition or Disease Intervention/Treatment Phase
  • Drug: Paracervical injection
  • Drug: prochlorperazine and diphenhydramine.(Standard Treatment)
Phase 2

Detailed Description

Headache is one of the most common presenting complaints in the emergency department.1 By the time patients with benign headaches present for treatment in the ED, they often have exhausted non-invasive treatments, and physicians are left with few therapeutic options.

Amongst the array of medications used by physicians to manage benign headache, dopamine antagonists have demonstrated the best efficacy in trials. A number of studies have demonstrated the efficacy of dopamine antagonists in treating migraine, tension, cluster-type, and other benign headaches2,3 Dopamine antagonists have shown superiority over opioids4, non-steroidal anti-inflammatory drugs5, triptans6, and anti-epileptics7. Prochlorperazine is probably the most studied and most commonly clinically utilized in this regard in the ED setting.

Despite the preponderance of evidence supporting the use of dopamine antagonists as first-line therapeutic agents in the ED management of benign headache, more than half of the 1.2 million patients treated in U.S. emergency departments for acute migraine are treated with opioids despite the known risks and recommendations to the contrary.12 In addition, there is tremendous variation in the medications chosen by ED physicians for managing benign headache.13 Most of these regimens involve administration of systemic medications that have considerable side effect profiles. Moreover, many of these headache cocktails require prolonged durations of treatment with sedative side effects. This results in prolonged ED lengths of stay that occupy valuable bed space in increasingly busy and crowded emergency departments.

A less well-known approach to managing benign headache is bilateral, paracervical, intramuscular injection of a long-acting anesthetic. The mechanism of action is not entirely understood, however it is postulated to involve neuronal pathways in the trigeminocervical complex thought to play a central role in headache physiology. This is similar in concept to the mechanism proposed for the occipital nerve blocks performed by neurologists.

Paracervical injection was first described by Mellick et al.8 This method has the advantage of ease of administration, favorable safety profile, lack of need for intravenous access, lack of sedative side effects, and swiftness of therapeutic response. In Mellick's case series, he treated 417 patients who presented with all manner of benign headaches with a 65% rate of complete relief of pain and a 20% rate of partial relief. Many patients had rapid relief of headache within 5 minutes and the remainder in less than 30 minutes. This study was limited by possible selection bias, given it is unclear why the specific patients enrolled were chosen for this treatment. The study was also limited by its observational nature and lack of a control group.

In recent years this procedure has gained popularity amongst emergency physicians, and it has been widely discussed in emergency medicine blogs and podcasts. Numerous online videos demonstrate the ease with which the procedure is performed by physicians and tolerated by patients. Many physicians have called for clinical trials to assess its efficacy.

The investigators therefore propose to study the use of paracervical injection as a novel approach to managing headache in the emergency department. This procedure has great potential, if efficacious, to provide a safe, rapidly effective, non-sedating treatment for headache that does not involve intravenous line placement and systemic medication administration. To date, there are no published trials that evaluate this technique in this setting. The investigators intend to compare the efficacy of paracervical injection to standard first-line therapy (intravenous prochlorperazine and diphenhydramine) for the treatment of benign headache of any etiology in the emergency department.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
108 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Intramuscular Paracervical Injection for Headache in the Emergency Department: A Randomized Controlled Trial
Actual Study Start Date :
Sep 15, 2020
Anticipated Primary Completion Date :
Sep 15, 2022
Anticipated Study Completion Date :
Sep 15, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Paracervical injection

1.5 mL of 0.5% bupivacaine will be will be injected bilaterally in the paraspinal musculature of the cervical spine.

Drug: Paracervical injection
1.5 mL of 0.5% bupivacaine will be will be injected bilaterally in the paraspinal musculature of the cervical spine.

Active Comparator: Standard treatment

Intravenous administration of prochlorperazine and diphenhydramine.

Drug: prochlorperazine and diphenhydramine.(Standard Treatment)
Intravenous administration of prochlorperazine and diphenhydramine.

Outcome Measures

Primary Outcome Measures

  1. Rate of symptom improvement [30 minutes]

    Patient asked if symptoms are improved enough for patient to be discharged to home.

Secondary Outcome Measures

  1. Reduction in pain scale [30 minutes]

    Pain scale measurement (1-10)

  2. Re-presentation for medical care [72 hours]

    Patient asked if re-presented for medical care in the previous 72 hours (yes/no)

  3. Headache recurrence [72 hours]

    Patient asked if headache recurred (yes/no)

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 64 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Age 18 to 64 years

  • Suspected diagnosis of benign or primary headache

Exclusion Criteria:
  • Treating attending physician is suspicious of a serious secondary cause of headache

  • History of brain disease, concussion, stroke, intracranial mass or tumor, hemorrhage, increased intracranial pressure, head trauma in last 2 weeks, status post intracranial surgery

  • History of neck disease, cervical spine or disc abnormality, history of vertebral or carotid artery dissection, torticollis, status post cervical spine surgery or hardware in place

  • Hypersensitivity or allergy to bupivacaine (amide anesthetics) or prochlorperazine (dopamine receptor antagonists)

  • Overlying signs of infection at site of injection (erythema, purulence, open skin)

  • History of extrapyramidal symptoms, dystonia, parkinsonism, tardive dyskinesia or neuroleptic malignant syndrome

  • Pregnancy

  • History of schizophrenia or bipolar disorder

  • Narcotic seeking patients as determined by the treating attending physician with optional assistance from medical record and online database review

  • Weight more than 150 kg or less than 40 kg

  • Received pain medication in the ED or less than 6 hours prior to enrollment

  • Temperature greater than 38 degrees Celcius

  • Previous enrollment

Contacts and Locations

Locations

Site City State Country Postal Code
1 Albert Einstein Medical Center Philadelphia Pennsylvania United States 19141

Sponsors and Collaborators

  • Christian Fromm, MD

Investigators

  • Principal Investigator: Christian Fromm, MD, Einstein Healthcare Network

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Christian Fromm, MD, Director of Clinical Trials, Albert Einstein Healthcare Network
ClinicalTrials.gov Identifier:
NCT04109885
Other Study ID Numbers:
  • 2019-173
First Posted:
Oct 1, 2019
Last Update Posted:
Dec 2, 2021
Last Verified:
Dec 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
Yes
Studies a U.S. FDA-regulated Device Product:
No
Product Manufactured in and Exported from the U.S.:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Dec 2, 2021