A Randomized, Sham-controlled Study of gammaCore ® (nVNS) for Prevention of Episodic Migraine

Inclusion Criteria

• Is between the ages of 18 and 75 years.
• Has been previously diagnosed with migraine (with or without aura) in accordance with the International Classification of Headache Disorders (ICHD)-3 Beta Classification criteria.
• Experience between 5 and 12 migraine days per month (over the last 4 months) with at least 2 of the migraines lasting more than 4 hours.
• Has age of onset of migraine less than 50 years old.
• Agrees not to use any migraine prevention treatments (including Botox injections) and/or medications (exclusive of medications taken for acute relief of migraine symptoms).
• Agrees to refrain from initiating or changing the type, dosage or frequency of any prophylactic medications for indications other than migraine that in the opinion of the clinician may interfere with the study objectives (e.g. antidepressant, anti convulsant, beta blockers, etc.).
• Agrees to use the gammaCore®-R device as intended, follow all of the requirements of the study including follow-up visit requirements, record required study data in the subject dairy, and other self-assessment questionnaires.
• Is able to provide written Informed Consent.

Exclusion Criteria

• Has a concomitant medical condition that will require oral or injectable steroids during the study.
• Has a history of any intracranial aneurysm, intracranial haemorrhage, brain tumour or significant head trauma.
• Has a structural abnormality at the gammaCore®-R treatment site (e.g lymphadenopathy previous surgery or abnormal anatomy).
• Has pain at the gammaCore®-R treatment site (e.g.dysesthesia, neuralgia and/or cervicalgia).
• Has other significant pain problem (e.g.cancer pain, fibromyalgia or other head or facial disorder) that in the opinion of the investigator may confound the study assessments
• Has know or suspected severe cardiac disease(e.g. symptomatic coronary artery disease, prior myocardial infarction, congestive heart failure (CHF)).
• Has known or suspected severe cerebrovascular disease, (e.g. prior stroke or transient ischemic attack, symptomatic carotid artery disease, prior carotid endarterectomy or other vascular neck surgery).
• Has an abnormal baseline Electrocardiogram (ECG) e.g. second and third degree heart block, prolonged QT interval, atrial fibrillation, atrial flutter, history of ventricular tachycardia or ventricular fibrillation, or clinically significant premature ventricular contraction).
• Has had a cervical vagotomy.
• Has uncontrolled high blood pressure (systolic >160 diastolic > 100 after 3 repeated measurements within 24 hours).
• Is currently implanted with an electrical and/or neurostimulator device (e.g. cardiac pacemaker or defibrillator, vagal neurostimulator, deep brain stimulator, spinal stimulator, bone growth stimulator cochlear implant, Sphenopalatine ganglion stimulator or Occipital nerve stimulator).
• Has been implanted with metal cervical spine hardware or has a metallic implant near the gammaCore®-R stimulation site.
• Has a known history of suspicion of secondary headache.
• Has a history of syncope (within the last five years).
• Has a history of seizures (within the last five years).
• Has a known or suspicion of substance abuse or addiction (within the last 5 years).
• Is using marijuana (including medical marijuana) for any indications, more than twice a month.
• Currently takes simple analgesics or non-steroidal anti-inflammatory drugs (NSAIDs) greater than 15 days per month or triptans, ergots or combined analgesics greater than 10 days per month for headaches or other body pain.
• Currently takes prescription opioids greater than 2 days per month for headaches or body pain.
• Has taken medications for migraine prophylaxis in the previous 30 days.
• Has previous diagnosis of medication overuse headache (MoH) , which has reverted to episodic migraine within the last 6 months.
• Meets the ICHD-3 Beta Classification criteria for chronic migraine (> 1