The purpose of this single arm, multi-center study is to confirm the safety and effectiveness of the AMPLATZER™ PFO Occluder in the post Approval Setting.
A maximum of 1214 adult subjects will be enrolled at up to 100 centers in the U.S. and Canada. Subjects will have follow-up at 1 month, 6 months, 12 months and annually thereafter through 5 years post implant.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
PREVENTION
Masking
NONE
Enrollment
1,214
Implantation of the AMPLATZER™ PFO Occluder in the PFO
Primary Effectiveness: 5 year rate of recurrent ischemic stroke
5 year rate of recurrent ischemic stroke
Time frame: Through 5 years
Primary Safety: Device or procedure related serious adverse events
Device or procedure related serious adverse events through 30 days
Time frame: Through 30 days post implant
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
University of Alabama at Birmingham
Birmingham, Alabama, United States
Heart Center Research, LLC
Huntsville, Alabama, United States
Chandler Regional Medical Center
Chandler, Arizona, United States
St. Joseph's Hospital and Medical Center
Phoenix, Arizona, United States
Scottsdale Healthcare Shea
Scottsdale, Arizona, United States
Pima Heart Physicians, PC
Tucson, Arizona, United States
UAMS Medical Center
Little Rock, Arkansas, United States
Kaiser Permanente Los Angeles Medical Center
Los Angeles, California, United States
USC University Hospital
Los Angeles, California, United States
Ronald Reagan UCLA Medical Center
Los Angeles, California, United States
...and 78 more locations