Understanding the Pathophysiology of Migraine Pain
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ClinicalTrials.gov Identifier: NCT03026101 |
Recruitment Status :
Enrolling by invitation
First Posted : January 20, 2017
Last Update Posted : February 7, 2023
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Migraine is the most common headache disorder, prevalent in 18% of females and 6% of males. Emergency room visits, physician consults, hospitalizations, medications, and indirect costs such as lost work days and decreased productivity place the global economic burden of migraines at over 20 billion dollars. It is prevalent in 28 million people in the US alone. Symptoms include unilateral, throbbing, debilitating headache pain accompanied by nausea, vomiting, photophobia, and phonophobia. Upwards of 75% of migraine patients have reduced functionability, have lost time at work, and 1/3 of patients require bed rest to manage the symptoms. The health-related impact on quality of life was comparable with that experienced by patients with congestive heart failure, hypertension, or diabetes.
While the burden of migraines on our society is clear, the pathophysiology of migraines remains largely unknown. The trigeminovascular system, including the external and internal carotid arteries and their associated sensory fibers which subserve the head have long been implicated in the pain and cutaneous allodynia experienced by migraine patients. Wolff in 1953, was the first to posit that migraine headache pain is the caused by dilation or circumferential expansion of the extracranial carotid artery. He demonstrated that migraineurs had twice the pulse amplitude in their external carotid arteries compared to control subjects and these changes were directly correlated to migraine symptoms. In a 2008 study, randomized migraineurs received nitroglycerin via peripheral IV or placebo for 20 minutes prior to obtaining magnetic resonance angiography (MRA). Nitroglycerin, a potent dilator of blood vessels, reliably induced migraine-like pain in up to 80% of patients, and transient dilation of vessels of up to nearly 40%, mostly in the extracranial vessels. Sumatriptan's efficacy in migraine relief provides further evidence for this theory, as it is a selective extracranial vessel constrictor which does not cross the blood brain barrier.
The goal of this current work is to utilize the direct, real-time angiography, which provides a high resolution map of vasculature, and demonstrate changes in vessel flow in patients who have migraine headache attacks. This information may guide therapeutic interventions in the future in order to better treat these migraine patients.
Condition or disease | Intervention/treatment | Phase |
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Migraine Disorders Migraine, Classic Migraine Without Aura | Other: Nitroglycerin | Not Applicable |

Study Type : | Interventional (Clinical Trial) |
Estimated Enrollment : | 20 participants |
Allocation: | N/A |
Intervention Model: | Single Group Assignment |
Masking: | None (Open Label) |
Primary Purpose: | Diagnostic |
Official Title: | Understanding the Role of the External Carotid Artery in the Pathophysiology of Migraine Pain |
Actual Study Start Date : | January 2017 |
Estimated Primary Completion Date : | December 2023 |
Estimated Study Completion Date : | December 2023 |

Arm | Intervention/treatment |
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Experimental: Migraine Intervention
Subjects who will be administered 200 micrograms of nitroglycerin once into branches of their external carotid artery to determine the role of dilation of this artery to cause migraine-like pain
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Other: Nitroglycerin
Intra-arterial adminstration to dilate external carotid artery branches to replicate migraine pain
Other Name: Nitrostat |
- Migraine [ Time Frame: 10 minutes ]The reporting of migraine-like pain after nitroglycerin administration
- Migraine log pre-procedure: severity measure [ Time Frame: 2 weeks ]Severity of migraines for 2 weeks prior to angiogram
- Migraine log pre-procedure: frequency measure [ Time Frame: 2 weeks ]Frequency of migraines for 2 weeks prior to angiogram
- Migraine log pre-procedure: quality measure [ Time Frame: 2 weeks ]Quality of migraines for 2 weeks prior to angiogram
- Migraine log pre-procedure: location measure [ Time Frame: 2 weeks ]Location of migraines for 2 weeks prior to angiogram
- Migraine log pre-procedure: alleviating factor measure [ Time Frame: 2 weeks ]Alleviating factors of migraines for 2 weeks prior to angiogram
- Migraine log pre-procedure: aggravating factor measure [ Time Frame: 2 weeks ]Aggravating factors of migraines for 2 weeks prior to angiogram
- Migraine log pre-procedure: associated symptom measure [ Time Frame: 2 weeks ]Associated symptoms of migraines for 2 weeks prior to angiogram
- Migraine log pre-procedure: therapies utilized measure [ Time Frame: 2 weeks ]Therapies utilized for migraines for 2 weeks prior to angiogram
- Artery dilation [ Time Frame: 10 minutes ]Enlargement of the diameter of the vessel of interest after nitroglycerin administration
- Migraine pain relief [ Time Frame: 20 minutes ]Relief of induced migraine pain with temporary balloon occlusion of the dilated artery. Standard pain medication will also be available for treatment
- Adverse reactions [ Time Frame: 6 hours ]Monitoring for retroperitoneal hematoma, vascular injury, infection, contrast reaction, worsening contralateral headache symptoms, new neurologic deficit peri-procedurally until discharge
- Migraine log follow-up post-procedure: severity measure [ Time Frame: 2 weeks ]Severity of migraines for 2 weeks post-angiogram
- Migraine log follow-up post-procedure: frequency measure [ Time Frame: 2 weeks ]Frequency of migraines for 2 weeks post-angiogram
- Migraine log follow-up post-procedure: quality measure [ Time Frame: 2 weeks ]Quality of migraines for 2 weeks post-angiogram
- Migraine log follow-up post-procedure: location measure [ Time Frame: 2 weeks ]Location of migraines for 2 weeks post-angiogram
- Migraine log follow-up post-procedure: alleviating factors measure [ Time Frame: 2 weeks ]Alleviating factors of migraines for 2 weeks post-angiogram
- Migraine log follow-up post-procedure: aggravating factor measure [ Time Frame: 2 weeks ]Aggravating factors of migraines for 2 weeks post-angiogram
- Migraine log follow-up post-procedure: associated factor measure [ Time Frame: 2 weeks ]Associated symptoms of migraines for 2 weeks post-angiogram
- Migraine log follow-up post-procedure: therapies utilized measure [ Time Frame: 2 weeks ]Therapies utilized for 2 weeks after angiogram until follow-up clinic visit

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Ages Eligible for Study: | 18 Years to 80 Years (Adult, Older Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
- Subjects with a documented diagnosis of migraine by a neurologist
- Subjects refractory to standard migraine therapy with persistent severe, debilitating symptoms
- Subjects without changes to their neurological exam within the preceding 6 months
- Migraines at least twice a month
- Migraines unique and distinguishable from other non-migraine headache pain
- Subjects must sign a consent form for both angiography and for participation in this study, and must be willing to undergo angiography for the evaluation of their symptoms
Exclusion Criteria:
- Subjects taking vasoactive drugs including epinephrine, norepinephrine, dopamine, dobutamine, isoprenaline, dopexamine, milrinone, amrinon, levosimendan, glucagon, phenylephrine, metaraminol, ephedrine, vasopressin, digoxin, and levothyroxine
- Subjects with underlying cardiac pathology including but not limited to coronary artery disease, heart attacks, or severe atherosclerosis,
- Subjects with severe pulmonary disease requiring supplemental oxygen therapy
- Subjects taking medications similar to nitroglycerin such as phosphodiesterase inhibitors
- Subjects with contraindications to nitroglycerin or calcium channel blocker use
- Subjects who have had coffee, tea, or alcohol in the 12 hours before the start of the angiogram
- Subjects having other headache conditions or pain syndromes
- Subjects with prior intracranial therapies or craniotomies for management of any intracranial lesions
- Subjects in whom the angiography demonstrates severe vessel tortuosity or stenosis, vasospasm not responsive to medical therapy, or abnormal communication between intracranial and extracranial vessels either in the past or during the study procedure
- Subjects who are not able to reliably report symptoms
- Subjects who do not consent to participate
- Subjects who are pregnant and children

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03026101
United States, New York | |
Montefiore Medical Center | |
Bronx, New York, United States, 10467 |
Principal Investigator: | David J Altschul, MD | Montefiore Medical Center |
Responsible Party: | David Altschul, Chief, The Leo M. Davidoff Department of Neurological Surgery Division of Cerebrovascular Neurosurgery, Montefiore Medical Center |
ClinicalTrials.gov Identifier: | NCT03026101 |
Other Study ID Numbers: |
2017-8335 |
First Posted: | January 20, 2017 Key Record Dates |
Last Update Posted: | February 7, 2023 |
Last Verified: | February 2023 |
Studies a U.S. FDA-regulated Drug Product: | No |
Studies a U.S. FDA-regulated Device Product: | No |
Migraine Disorders Migraine without Aura Migraine with Aura Headache Disorders, Primary Headache Disorders |
Brain Diseases Central Nervous System Diseases Nervous System Diseases Nitroglycerin Vasodilator Agents |