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Research
Treating Atrial Septal Defects with Amplatzer
Closure of Atrial Septal Defects with the Amplatzer® Septal Occluder Post Market Study
Protocol Description
The purpose of this multi-center study is to gather more information about how effective the Amplatzer® Septal Occluder is at closing atrial septal defects (ASD). An ASD is an opening in the wall that divides the upper chamber of the heart. The Amplatzer device is an expandable disc that is placed into the heart via cardiac catheterization.
Eligibility Criteria
Subject to certain baseline testing, eligible candidates include male and female babies and children diagnosed with an ASD condition that would benefit from closure with a septal occluder.
Boys: All ages
Girls: All ages
Requirements
Following baseline testing for eligibility, patients will receive the implant procedure through the catheterization lab in a non-surgical procedure. During the first 6 months following the procedure, patients may be required to take aspirin and antibiotics. Additional testing may be required over the 2-year follow-up period.
Visits: Requires hospital visit
Duration: 2 years
Status: Enrolls Only from Current Patient Cases
Source of Support
AGA Medical Corporation
Primary Investigator(s)
Jacqueline Kreutzer, MD, FACC, FSCAI
Contact Information
For information, please contact:
Jane Luce, MPH, CHES
412-692-6762
Last Update
April 27, 2011
April 27, 2011

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