New study tracks amulet Device's Real-World success in preventing strokes
NCT ID NCT05997446
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study observes over 600 people with atrial fibrillation who received the Amulet device to close a part of the heart called the left atrial appendage. The goal is to see how well the device prevents strokes and bleeding in everyday medical practice. Participants are followed for 24 months to track safety and effectiveness.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Arizona Arrhythmia Research
Phoenix, Arizona, 85016, United States
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Arkansas Heart Hospital
Little Rock, Arkansas, 72211, United States
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Baptist Medical Center
Jacksonville, Florida, 32207, United States
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Baylor All Saints Medical Center at Fort Worth
Fort Worth, Texas, 76104, United States
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Bryan Heart
Lincoln, Nebraska, 68506, United States
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CHI Health Creighton University Medical Center-Bergan Mercy
Omaha, Nebraska, 68124, United States
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Cardiovascular Research Institute of Kansas
Wichita, Kansas, 67226, United States
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Heart Rhythm Associates
Shenandoah, Texas, 77380, United States
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Kansas City Cardiac Arrhythmia Research Foundation
Overland Park, Kansas, 66211, United States
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New York University Hospital
New York, New York, 10016, United States
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PERC - O'Fallon
O'Fallon, Illinois, 62269, United States
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Pinnacle Health System
Mechanicsburg, Pennsylvania, 17150, United States
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Providence Hospital
Southfield, Michigan, 48075, United States
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Trident Medical Center
Charleston, South Carolina, 29406, United States
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Usman R. Siddiqui, MD
Winter Park, Florida, 32792, United States
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Vanderbilt Heart & Vascular Institute
Nashville, Tennessee, 37232, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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