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Paracervical Injection for Headache in the Emergency Department

Primary Purpose

Headache Disorders, Primary, Pain Management, Emergency Department

Status
Active
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Paracervical injection
prochlorperazine and diphenhydramine.(Standard Treatment)
Sponsored by
Christian Fromm, MD
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Headache Disorders, Primary

Eligibility Criteria

18 Years - 64 Years (Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • Albert Einstein Medical Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Paracervical injection

Standard treatment

Arm Description

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

Intravenous administration of prochlorperazine and diphenhydramine.

Outcomes

Primary Outcome Measures

Rate of symptom improvement
Patient asked if symptoms are improved enough for patient to be discharged to home.

Secondary Outcome Measures

Reduction in pain scale
Pain scale measurement (1-10)
Re-presentation for medical care
Patient asked if re-presented for medical care in the previous 72 hours (yes/no)
Headache recurrence
Patient asked if headache recurred (yes/no)

Full Information

First Posted
September 27, 2019
Last Updated
May 23, 2023
Sponsor
Christian Fromm, MD
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1. Study Identification

Unique Protocol Identification Number
NCT04109885
Brief Title
Paracervical Injection for Headache in the Emergency Department
Official Title
Intramuscular Paracervical Injection for Headache in the Emergency Department: A Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
September 15, 2020 (Actual)
Primary Completion Date
September 15, 2023 (Anticipated)
Study Completion Date
September 15, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Christian Fromm, MD

4. Oversight

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

5. 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.
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Headache Disorders, Primary, Pain Management, Emergency Department

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
108 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Paracervical injection
Arm Type
Experimental
Arm Description
1.5 mL of 0.5% bupivacaine will be will be injected bilaterally in the paraspinal musculature of the cervical spine.
Arm Title
Standard treatment
Arm Type
Active Comparator
Arm Description
Intravenous administration of prochlorperazine and diphenhydramine.
Intervention Type
Drug
Intervention Name(s)
Paracervical injection
Intervention Description
1.5 mL of 0.5% bupivacaine will be will be injected bilaterally in the paraspinal musculature of the cervical spine.
Intervention Type
Drug
Intervention Name(s)
prochlorperazine and diphenhydramine.(Standard Treatment)
Intervention Description
Intravenous administration of prochlorperazine and diphenhydramine.
Primary Outcome Measure Information:
Title
Rate of symptom improvement
Description
Patient asked if symptoms are improved enough for patient to be discharged to home.
Time Frame
30 minutes
Secondary Outcome Measure Information:
Title
Reduction in pain scale
Description
Pain scale measurement (1-10)
Time Frame
30 minutes
Title
Re-presentation for medical care
Description
Patient asked if re-presented for medical care in the previous 72 hours (yes/no)
Time Frame
72 hours
Title
Headache recurrence
Description
Patient asked if headache recurred (yes/no)
Time Frame
72 hours

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
64 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Christian Fromm, MD
Organizational Affiliation
Einstein Healthcare Network
Official's Role
Principal Investigator
Facility Information:
Facility Name
Albert Einstein Medical Center
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19141
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No

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Paracervical Injection for Headache in the Emergency Department

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