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About
Rimegepant (Nurtec) is an orally administered small molecule CGRP receptor antagonist with efficacy in the acute treatment of migraine. Rizatriptan benzoate (MAXALT), is a selective 5-hydroxytryptamine1B/1D (5-HT1B/1D) receptor agonist. Rizatriptan binds with high affinity to human cloned 5-HT1B and 5-HT1D receptors which leads to activation of these receptors results in cranial vessel constriction, inhibition of neuropeptide release and reduced transmission in trigeminal pain pathways with resultant relieve of the headache.
Teh investigators hypothesize that the administration of Rimegepant ODT would provide better analgesic efficacy than Rizatriptan ODT with respect to analgesic efficacy at 60 min and 120 minutes in ED patients with acute headache.
This is a prospective, randomized, double-blind superiority trial evaluating and comparing analgesic efficacy and safety of Rimegepant ODT 75 mg to Rizatriptan ODT 10 mg in adult patients presenting to the Emergency Department of Maimonides Medical Center with acute migraine headache.
Full description
This is a prospective, randomized, double-blind superiority trial evaluating and comparing analgesic efficacy and safety of Rimegepant ODT 75 mg to Rizatriptan ODT 10 mg in adult patients presenting to the ED of Maimonides Medical Center with acute migraine headache.
The investigators will conduct the study in the emergency department of Maimonides Medical Center, an urban emergency department that receives over 120,000 adult visits annually. The emergency department is staffed on weekdays by salaried, trained, bilingual (English and Spanish) research associates who execute research studies under the supervision of the principal investigators. Adult patients between ages of 18 and 65 presenting to the ED with an acute exacerbation of a migraine without aura as defined by the International Classification of Headache Disorders, 3rd edition criteria for migraine without aura or for probable migraine without aura, with an initial pain score of 5 or more on a standard 11- point (0 to 10) numeric rating scale, and requiring oral analgesia as determined by the treating attending physician will be eligible for participation. Subjects' screening and enrollment will be performed by study investigators and research assistants. All patients will be enrolled at various times of the day when study investigators will be available for patient enrollment and an ED pharmacist will be available for medication preparation.
Each patient will be approached by research associates for acquisition of written informed consent and Health Insurance Portability and Accountability Act authorization after being evaluated by the treating emergency physician and determined to meet study eligibility criteria. When English will not be the participant's primary language, a language- appropriate consent form will be used and non-investigator, hospital-employed, trained interpreters or licensed telephone interpreter will assist in acquisition of informed consent. Baseline pain score will be determined with an 11-point numeric rating scale (0 to 10), described to the patient as "no pain" being 0 and "the worst pain imaginable" being 10.
Research associates will ascertain the subject's headache level every 30 minutes after medication administration for up to 120 minutes. If enrolled subjects required more pain medication at or after one hour had elapsed, they will be given additional medication at the discretion of the treating physician.
The research team will be contacting all of research subjects by telephone 24 hours after ED discharge to ascertain headache status, satisfaction with treatment, and presence of adverse events.
All data will be recorded on data collection sheets, including patients' sex, demographics, medical history, and vital signs, and entered into SPSS (version 24.0; IBM Corp) by the research manager. Confirmation of written consent acquisition for all participants, and statistical analyses will be conducted by the institutional biostatistician who will work independently of any data collection.
As a primary measure of headache intensity, the investigators utilized a standard, validated, and reproducible 11-point numerical rating scale (NRS). This scale uses patients' responses in assigning their pain a number between 0 and 10, with 0 representing no pain and ten representing the worst pain imaginable. Secondary measurement scales included a standard four-point pain intensity categorical scale, in which patients describe their pain as "severe", "moderate", "mild", or "none" and a four-point functional disability scale, in which patients describe their headache-related disability as severe ("cannot get up from bed or stretcher"), moderate ("great deal of difficulty doing what I usually do and can only do very minor activities" ), mild ("little bit of difficulty doing what I usually do"), or none. These scales will be used in accordance with the recommendation by the International Headache Society for use in migraine research.
One hour after medication administration, the investigators will ask all of enrolled patients if they needed more medication for pain. Lastly, we will assess enrolled patients' satisfaction (efficacy and tolerability of the study drug) with treatment by asking each of them, 24 hours after enrollment, whether they would want to receive the same medication the next time they visited the ED with an acute migraine.
The primary outcome for this study will be a comparison of change in numerical rating scale score between baseline and one hour between two investigational arms.
Secondary outcomes will include:
Enrollment
Sex
Ages
Volunteers
Inclusion criteria
Exclusion criteria
Allergy to Rimegepant or Rizatriptan
Pregnancy and breastfeeding
Unstable vital signs
Inability to provide consent
Suspicion for disease process other than migraine (those requiring emergent brain imaging, with a temperature of 100.4 °F, with objective neurologic findings, secondary headache (an "organic" headache))
Ischemic coronary artery disease (angina pectoris, history of myocardial infarction), coronary artery vasospasm (including Prinzmetal's angina)
History of stroke or transient ischemic attack
Peripheral vascular disease
Ischemic bowel disease,
Uncontrolled hypertension
Use of another 5-HT1 agonist, ergotamine-containing medications, or ergot-type medications (methylsergide)
Hemiplegic or basilar migraine
Concurrent administration or recent discontinuation (within 2 weeks) of a MAO-A inhibitors
Current use of Rimegepant as a prophylactic
Severe Nausea and Vomiting
Severe headache requiring immediate intervention
Severe hepatic impairment
If taking any of the following medications (contraindications):
Primary purpose
Allocation
Interventional model
Masking
80 participants in 2 patient groups
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Central trial contact
Antonios Likourezos, MPH; Sergey Motov, MD
Data sourced from clinicaltrials.gov
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