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Magnesium Versus Prochlorperazine Versus Metoclopramide for Migraines

A Randomized, Placebo-Controlled, Double-Blind Study of the Effects of Magnesium Compared to Conventional Therapy on Acute Migraine

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05967442
Acronym
MAGraine
Enrollment
157
Registered
2023-08-01
Start date
2019-08-23
Completion date
2023-04-06
Last updated
2024-10-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Migraine, Headache

Keywords

magnesium, migraine, headache

Brief summary

This investigation describes a proposed clinical trial that will evaluate the relative efficacy of intravenous magnesium sulfate for the treatment of migraine compared to intravenous metoclopramide (Reglan) and intravenous prochlorperazine (Compazine) in the treatment of acute headache and migraine in adult patients. The ultimate objective will be clinical application of these drugs in the emergency department for the treatment of acute headache and migraine. The two phenothiazines (metoclopramide and prochlorperazine) have been routinely utilized in the treatment of acute headache and migraine in the emergency department setting. Per the 2017 American Headache Society guidelines, both intravenous metoclopramide and intravenous procholorperazine are recommended as clinicians should offer agents with level B evidence. Of note, there are no agents with level A evidence purported by this guideline for acute management of migraine. The same guideline offers no recommendation can be made regarding the role of intravenous magnesium for adults who present to the ED with acute migraine. However intravenous magnesium may be of benefit to patients who present with migraine with aura. Multiple trials have evaluated intravenous magnesium's safety and efficacy in the management of acute migraine. These have demonstrated the tolerability of intravenous magnesium on a with breadth of patients. Most commonly the primary adverse event was flushing which self-resolved. No cases of hypotension were reported. None of these study agents have been withdrawn from the market.

Detailed description

Migraine or severe headache affected one-fifth of women and one-tenth of men in 2015 and is one of the leading causes of disability in the world. Over one million visits to emergency departments (ED) in the US are due to migraines. Migraine, previously believed to be a vascular disorder, is caused by inflammation due to vasodilation in the meninges secondary to the release of vasoactive neuropeptides by stimulation of the trigeminal nerve. This inflammation can result in symptoms such as headache, nausea, vomiting, dizziness, photophobia and phonophobia. Despite migraine being a common disorder, there has yet to be a cure. Several classes of medications have been studied for the treatment of migraine. Recently, conventional therapy has shifted to the use of antidopaminergics including prochlorperazine, metoclopramide and haloperidol, nonsteroidal anti-inflammatory drugs (NSAIDs) such as ibuprofen and naproxen, and triptans, sumatriptan being the most commonly utilized. 5Although intravenous opioids have historically been the most common treatment for migraines, their use has fallen out of favor due to their association with increased recurrence of headaches and ED visits, abuse potential, and most recently severe intravenous opiate shortage. Alternative treatments include ketamine, propofol, dihydroergotamine and magnesium. Magnesium is an intracellular cation that has been associated with both the function of serotonin and regulation of vascular tone, which are both mechanisms that implicate its role in the treatment of migraine. Intravenous magnesium sulfate has been studied as a treatment for migraine compared to placebo, metoclopramide and prochlorperazine. These studies have shown that magnesium is well-tolerated with a good safety profile and may be efficacious in the treatment of migraine. Metoclopramide, prochlorperazine and magnesium have been recommended in clinical practice guidelines and have become routine standard of care for treatment of migraine in this emergency department. However, no trial has evaluated these modalities simultaneously in the same population. The purpose of our study is to compare the relative efficacy for magnesium, metoclopramide, and prochlorperazine in the treatment of headache and migraine. Via monthly block randomization, patients will be given one of three guideline recommended study drugs. Allocation will be concealed by a pharmacist (not participating in the rest of the study) solely designated to choose which drug will be the assigned study drug for each month. The pharmacists, physicians, and nurses participating in administration of the medications will be blinded to which drug is being administered during each month. Metoclopramide, prochlorperazine and magnesium have been recommended in clinical practice guidelines and have become routine standard of care for treatment of migraine in this emergency department. All three study drugs will be stored in the investigational medication refrigerator located in the main pharmacy. A pharmacist on duty in the emergency department will obtain the medication from the refrigerator and deliver it to the bedside nurse who is actively caring for the patient after an order from the physician. The primary outcome of this study will be mean change in pain from baseline to 30 minutes after initiation of infusion (as defined on a 11-point Numeric Rating Scale. Secondary endpoints include mean change in pain from baseline to 60 minutes and 120 minutes after initiation of infusion (as defined on a 11-point Numeric Rating Scale), time to emergency department discharge, and adverse effects due to administration of study drug (hypotension, flushing, akathisia, dystonia, nausea, vomiting, dizziness, drowsiness, other self-reported adverse effects).

Interventions

DRUGMagnesium Sulfate

Magnesium Sulfate 2gm in 50ml D5W over 20 minutes

Metoclopramide 10mg in 50ml D5W over 20 minutes

DRUGProchlorperazine (Compazine) Injection

Prochlorperazine 10mg in 50ml D5W over 20 minutes

Sponsors

Wake Forest University Health Sciences
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Age \> 18 years or older * Able to provide informed consent * Primary diagnosis of headache or migraine * Between October 1, 2018 to April 1, 2020 * Presenting to Advocate Christ Medical Center emergency department and meet clinical assessment per physician

Exclusion criteria

* Pregnancy defined as a positive urine HCG * Stated history of renal impairment * Allergy or sensitivity to any study drugs * Concomitant treatment at the time of study drug administered in the emergency department * Patients with a history of this study participation

Design outcomes

Primary

MeasureTime frameDescription
30 Minute Pain Score30 minutes after initiationScores range from 0-10. A higher score, denotes more pain

Secondary

MeasureTime frameDescription
Length of StayFrom time of arrival to time of discharge.Emergency Department Length of stay. Measured from time of arrival to time of discharged documented in the electronic medical record.
Need for Rescue AnalgesiaFrom time of arrival to time of discharge.Percentage of participants who had necessity for rescue analgesics after study drug administration

Countries

United States

Participant flow

Participants by arm

ArmCount
Magnesium
Magnesium Sulfate: Magnesium Sulfate 2gm in 50ml D5W over 20 minutes
61
Metoclopramide
Metoclopramide 10mg in 50ml D5W over 20 minutes Metoclopramide 10mg: Metoclopramide 10mg in 50ml D5W over 20 minutes
44
Prochlorperazine
Prochlorperazine in 50ml D5W over 20 minutes Prochlorperazine (Compazine) Injection: Prochlorperazine 10mg in 50ml D5W over 20 minutes
52
Total157

Baseline characteristics

CharacteristicMagnesiumMetoclopramideProchlorperazineTotal
Age, Continuous34 years37.5 years37.5 years36 years
Ethnicity (NIH/OMB)
Hispanic or Latino
6 Participants5 Participants9 Participants20 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
55 Participants39 Participants42 Participants136 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
0 Participants0 Participants1 Participants1 Participants
Sex: Female, Male
Female
44 Participants33 Participants46 Participants123 Participants
Sex: Female, Male
Male
17 Participants11 Participants6 Participants34 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
EG002
affected / at risk
deaths
Total, all-cause mortality
0 / 610 / 440 / 52
other
Total, other adverse events
0 / 610 / 440 / 52
serious
Total, serious adverse events
0 / 610 / 440 / 52

Outcome results

Primary

30 Minute Pain Score

Scores range from 0-10. A higher score, denotes more pain

Time frame: 30 minutes after initiation

Population: Full cohort

ArmMeasureValue (MEDIAN)
Magnesium30 Minute Pain Score3 score on a scale
Metoclopramide30 Minute Pain Score3 score on a scale
Prochlorperazine30 Minute Pain Score3 score on a scale
Secondary

Length of Stay

Emergency Department Length of stay. Measured from time of arrival to time of discharged documented in the electronic medical record.

Time frame: From time of arrival to time of discharge.

ArmMeasureValue (MEDIAN)
MagnesiumLength of Stay325 minutes
MetoclopramideLength of Stay308 minutes
ProchlorperazineLength of Stay332 minutes
Secondary

Need for Rescue Analgesia

Percentage of participants who had necessity for rescue analgesics after study drug administration

Time frame: From time of arrival to time of discharge.

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
MagnesiumNeed for Rescue Analgesia26 Participants
MetoclopramideNeed for Rescue Analgesia15 Participants
ProchlorperazineNeed for Rescue Analgesia17 Participants

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026