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Completed

NCT Number: NCT01138150

Ictal and Interictal Inflammatory Markers in Migraine

The purpose of this study is to evaluate blood levels of several proteins that may be altered in the inflammation associated with migraine headaches. These blood levels will be evaluated in individuals during an acute migraine attack and compared to their levels when pain free. The investigators study hypothesis is that the pro inflammatory proteins in the blood will be greater than the levels of these proteins when evaluated during a pain free period.

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Key information

Age range

18 year–55 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

The Johns Hopkins Bayview Headache Center

Baltimore, Maryland, 21224, United States

About this study

Migraine is a common, chronic disorder, which presents with recurrent episodes of disabling headache and affects approximately 12% of American adults.1,2 No biomarkers exist to identify episodic or chronic migraine sufferers; and the diagnosis relies solely on clinical criteria. Further the full pathophysiology of migraine has not been fully delineated, although our understanding of migraine pathophysiology has dramatically improved over the past 15 years. Current theories suggest that migraine is a neurovascular disorder, with the pain of migraine a result of the release of inflammatory neuropeptides from nerve endings in the activated trigeminal system (neurogenic inflammation), ultimately resulting in vasodilation, plasma extravasation and mast cell degranulation.3-6 Several inflammatory markers have been implicated in the pathway resulting in the neurogenic inflammation of migraine including calcitonin gene related peptide (CGRP), substance P (SP), neurokinin A, and multiple cytokines such as interleukin (IL) -1, IL-6 and tumor necrosis-α (TNF-α).5,7-10 More recent research supports that the odds of migraine are increased in those who are obese and that several adipose tissue derived cytokines (adipocytokines) may contribute to the neurogenic inflammation of migraine, including leptin and adiponectin. In one small pilot study of 33 participants evaluating chronic and episodic migraineurs as compared to controls, adiponectin (an adipocytokine) was significantly elevated in chronic migraineurs as compared to controls. A second study reported low levels of another adipocytokine, leptin in episodic migraineurs. However, all of these studies have evaluated only 3 to 4 of cytokines at the same time point and 11 none have evaluated adipocytokines during an acute attack. We hypothesize that obesity-related cytokines contribute to the neurogenic inflammation of migraine and have the potential be useful as biomarkers for episodic and chronic migraine as well as new drug targets for the treatment of migraine. To this end we propose to evaluate serum levels of obesity-related cytokines in migraineurs, ictally (during an acute migraine attack), following treatment with sumatriptan/naproxen sodium (Treximet®) and interictally (at baseline) when pain free.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age greater than 18 years of age, migraine

Exclusion criteria

  • Pregnant or breast-feeding women, presence of cardiovascular or cerebrovascular disorders as well as any known inflammatory, infectious, metabolic, thyroid, renal, cardiovascular or gastrointestinal diseases

Treatment and study plan

Treximet

Drug

One tablet of sumatriptan 85 mg and naproxen sodium 500 mg will be given upon subject presentation with an acute migraine attack and after blood levels have been drawn.

Other names: The brand name of sumatriptan/naproxen sodium is Treximet.

Placebo

Drug

One tablet of a sugar pill will be given upon subject presentation with an acute migraine attack and after blood levels have been drawn.

Other names: Sugar Pill

Primary outcomes

  1. Change in the Total Serum Adiponectin (T-ADP)

    Time frame: 30 minutes after treatment, 60 minutes after treatment, 120 minutes after treatment

    Change in total serum adiponectin after treatment in responders and non responders

Secondary outcomes

  1. High Molecular Weight (HMW)-Adiponectin (ADP)

    Time frame: 30 minutes after treatment, 60 minutes after treatment, 120 minutes after treatment

    serum HMW-ADP levels after treatment in responders and non responders

  2. Middle Molecular Weight (MMW)-ADP

    Time frame: 30 minutes after treatment, 60 minutes after treatment, 120 minutes after treatment

    serum MMW-ADP levels after treatment in responders and non responders

  3. Low Molecular Weight (LMW)-ADP

    Time frame: 30 minutes after treatment, 60 minutes after treatment, 120 minutes after treatment

    serum LMW-ADP levels after treatment in responders and non responders

  4. High Molecular Weight (HMW): T-ADP

    Time frame: 30 minutes, 60 minutes, 120 minutes after treatment

    serum HMW:T-ADP levels after treatment in responders and non responders

  5. Low Molecular Weight (LMW):Total (T)-ADP

    Time frame: 30 minutes after treatment, 60 minutes after treatment, 120 minutes after treatment

    serum LMW:T-ADP levels after treatment in responders and non responders

  6. Leptin

    Time frame: 30 minutes after treatment, 60 minutes after treatment, 120 minutes after treatment

    serum leptin levels after treatment in responders and non responders

  7. Resistin

    Time frame: 30 minutes after treatment, 60 minutes after treatment, 120 minutes after treatment

    serum resistin levels after treatment in responders and non responders

Sponsors and collaborators

Lead sponsor

Johns Hopkins University

Other

Collaborators

  • The Cleveland Clinic
  • University of Toledo Health Science Campus

Registry information

Important dates

Study start
2009
Primary completion
2013
Study completion
2013
First posted
Jun 7, 2010
Registry last updated
Oct 6, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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