Brain pacemaker tested for years to tame severe seizures
NCT ID NCT03900468
Summary
This study is following 140 adults with severe epilepsy who have received a surgically implanted brain stimulation device. The goal is to collect three years of real-world data to see how well the device continues to reduce seizure frequency and to monitor for any long-term safety issues. Participants are adults whose seizures have not been controlled by at least three different medications.
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Contacts and locations
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Locations
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Cleveland Clinic
Cleveland, Ohio, 44195, United States
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Emory University Hospital
Atlanta, Georgia, 30303-3049, United States
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Fakultni nemocnice u sv. Anny v Brně/ Milan Brazdil
Brno, 656 91, Czechia
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Indiana University Health Neuroscience Center
Indianapolis, Indiana, 46202-2274, United States
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Massachusetts General Hospital
Boston, Massachusetts, 02114, United States
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Mayo Clinic (Rochester MN)
Rochester, Minnesota, 55905, United States
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Rush University Medical Center
Chicago, Illinois, 60612, United States
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Stanford Hospital & Clinics
Stanford, California, 94305, United States
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The Ohio State University
Columbus, Ohio, 43210, United States
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Thomas Jefferson University Hospital
Philadelphia, Pennsylvania, 19107, United States
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University of California Los Angeles (UCLA)
Los Angeles, California, 90095-1406, United States
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University of California San Francisco UCSF Medical Center
San Francisco, California, 94143, United States
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University of Kansas Medical Center
Kansas City, Kansas, 66160-8500, United States
Conditions
Explore the condition pages connected to this study.