The purpose of this two arm controlled double-blind study is to determine the safety and effectiveness of PFO closure (closing a hole in the wall of the heart) in reducing the frequency of migraine headaches, in patients who experience migraine headaches and have a PFO, compared to medical therapy alone.
Migraine headache is a neurological disorder characterized by chronic and disabling headache. Approximately 10-12% of humans, comprising some 28 million Americans, suffer from this disorder. Despite continual advances in medical management of migraine, many sufferers continue to experience frequent and disabling attacks despite appropriate medical therapy. Preventative medications, such as anti-epileptic drugs, anti-depressants, and beta-blockers, while effective for many patients, have side-effect profiles that preclude use in many patients. In the past decade, there has been growing evidence that patients with migraine, particularly those with aura, are more likely to have a patent foramen ovale. A patent foramen ovale (PFO) is a persistent, flap-like opening in the wall of the heart, between the right and left atrium. Typically, this opening closes shortly after birth, however, in some people, it remains open. While there is currently no proof for cause-effect relationship, several recent studies have confirmed a strong association between the presence of PFO and migraine with aura. Comparison: This clinical study will compare PFO closure with medical therapy alone for the treatment of migraine headaches.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
168
PFO Closure with Premere investigational device.
Medical management with current medications per standard of care by personal physician.
Primary Endpoint 1: Effectiveness
Time frame: 12 months
The primary effectiveness measure is the decrease in the frequency of migraine headaches.
Time frame: monthly
The primary safety endpoint is the rate of major complications
Time frame: monthly
Secondary Endpoint 1: Effect of Aura
Time frame: on-going
Secondary Endpoint 2: Assessment of Procedural Success and Long-Term Device Performance
Time frame: Five years
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Advanced Neurosciences Research, LLC
Fort Collins, Colorado, United States
Hartford Headache Center
East Hartford, Connecticut, United States
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Washington D.C., District of Columbia, United States
Jacksonville Center for Clinical Research
Jacksonville, Florida, United States
Neurology Associates
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...and 27 more locations