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Effect of Septal Closure of Atrial PFO on Events of Migraine With Premere: ESCAPE Migraine Trial
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.
Age
18 - 70 years
Sex
ALL
Healthy Volunteers
No
Mayo Clinic Hospital
Scottsdale, Arizona, United States
Newport Beach Clinical Research Associates, Inc.
Newport Beach, California, United States
Sutter Institute for Medical Research
Sacramento, California, United States
Alpine Clinical Research Center
Boulder, Colorado, United States
Mile High Research Center
Denver, Colorado, United States
Advanced Neurosciences Research, LLC
Fort Collins, Colorado, United States
Hartford Headache Center
East Hartford, Connecticut, United States
Medstar Clinical Research at Washington Hospital Center
Washington D.C., District of Columbia, United States
Jacksonville Center for Clinical Research
Jacksonville, Florida, United States
Neurology Associates
Maitland, Florida, United States
Start Date
November 1, 2005
Primary Completion Date
March 1, 2012
Completion Date
March 1, 2012
Last Updated
February 4, 2019
168
ACTUAL participants
PFO Closure with Premere investigational device.
DEVICE
Medical management/current medications per standard of care by personal physician.
DRUG
Lead Sponsor
Abbott Medical Devices
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT05690737