AMPLATZER™ PFO Occluder: Implantation of the AMPLATZER™ PFO Occluder in the PFO
Study summary
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.
Eligibility
Sex
ALL
Min age
18 Years
Max age
60 Years
Healthy volunteers
No
Inclusion Criteria:
• Subjects with a PFO who have had an ischemic stroke within the last 547 days
Exclusion Criteria:
* Atherosclerosis or other arteriopathy of the intracranial and extracranial vessels associated with a ≥ 50% lumen diameter supplying the involved lesion
* Intra-cardiac thrombus or tumor
* Documented evidence of venous thrombus in the vessels through which access to the PFO is gained
* Acute or recent (within 6 months prior to consent) myocardial infarction or unstable angina
* Left ventricular aneurysm or akinesis
* Mitral valve stenosis or severe mitral regurgitation requiring intervention irrespective of etiology
* Aortic valve stenosis (mean gradient \>40 mmHg) or severe aortic valve regurgitation
* Mitral or aortic valve vegetation or prosthesis
* Aortic arch plaques protruding greater than 4mm into the aortic lumen
* Left ventricular dilated cardiomyopathy with depressed left ventricular ejection fraction (LVEF less than 35%)
* Subjects with other source of right to left shunts, including an atrial septal defect and/or fenestrated septum
* Chronic, persistent, or paroxysmal atrial fibrillation or atrial flutter
* Pregnancy at the time of implant
* Age less than 18 years or greater than 60 years at time of consent
* Active endocarditis or other untreated infections
* Organ failure (kidney, liver or lung). Kidney failure: Poor urine output of less than 1 cc/kg/hr with elevated BUN levels (above the normal reference range for the laboratory at the investigational site). Liver failure: Liver enzymes outside the normal reference range for the laboratory at the investigational site: poor liver function as assessed by elevated PT (above the normal reference range for the laboratory at the investigational site) and low total protein and albumin (below the normal reference range for the laboratory at the investigational site). Lung failure: Respiratory failure is retention of carbon dioxide more than 60 mmHg, poor oxygenation with oxygen tension less than 40 mmHg in room air or the need for assisted ventilation.
* Uncontrolled hypertension defined as sustained elevated systemic blood pressure to more than 160/90 mmHg with medications
* Uncontrolled diabetes defined as continued elevated glucose levels in spite of administration of insulin/levels of more than 200 mg with presence of glucose in the urine
* Diagnosis of lacunar infarct probably due to intrinsic small vessel as qualifying stroke event Definition: Ischemic stroke in the distribution of a single, small deep penetrating vessel in a patient with any of the following: 1) a history of hypertension (except in the first week post stroke); 2) history of diabetes mellitus; 3) Age \>/= 50; or 4) MRI or CT shows leukoaraiosis greater than symmetric, well-defined periventricular caps or bands (European Task Force on Age-Related White Matter Changes rating scale score \> 0)
* Arterial dissection as cause of stroke
* Subjects who test positive with one of the following hypercoagulable states; Anticardiolipin Ab of the IgG or IgM (≥30), Lupus anticoagulant, B2-glycoprotein-1 antibodies (≥30) or persistently elevated homocysteine (\>20)
* Unable to take antiplatelet therapy
* Anatomy in which the AMPLATZERTM PFO Occluder device size required would interfere with intracardiac or intravascular structures such as valves or pulmonary veins
* Vasculature, through which access to the PFO is gained, is inadequate to accommodate the appropriate sheath size
* Malignancy or other illness where life expectancy is less than 2 years
* Subjects who will not be available for follow-up for the duration of the trial
* Inability to obtain Informed Consent from patient
* Index stroke of poor outcome (modified Rankin score greater than 3)
Primary outcome measure(s)
Primary Effectiveness: 5 year rate of recurrent ischemic stroke — Through 5 years 5 year rate of recurrent ischemic stroke
Primary Safety: Device or procedure related serious adverse events — Through 30 days post implant Device or procedure related serious adverse events through 30 days
Trial sites (88)
Facility
City
Region
Status
University of Alabama at Birmingham
Birmingham
Alabama
Heart Center Research, LLC
Huntsville
Alabama
Chandler Regional Medical Center
Chandler
Arizona
St. Joseph's Hospital and Medical Center
Phoenix
Arizona
Scottsdale Healthcare Shea
Scottsdale
Arizona
Pima Heart Physicians, PC
Tucson
Arizona
UAMS Medical Center
Little Rock
Arkansas
Kaiser Permanente Los Angeles Medical Center
Los Angeles
California
USC University Hospital
Los Angeles
California
Ronald Reagan UCLA Medical Center
Los Angeles
California
Sutter Medical Center
Sacramento
California
San Diego Cardiac Center
San Diego
California
University of California at San Francisco
San Francisco
California
Stanford University Medical Center
Stanford
California
Los Robles Hospital and Medical Center
Thousand Oaks
California
University of Colorado Hospital
Aurora
Colorado
Memorial Hospital of Colorado Springs
Colorado Springs
Colorado
Denver Heart
Denver
Colorado
South Denver Cardiology Associates PC
Littleton
Colorado
MedStar Washington Hospital Center
Washington D.C.
District of Columbia
St. Vincent's Medical Center
Jacksonville
Florida
Baptist Medical Center
Jacksonville
Florida
First Coast Cardiovascular Institute
Jacksonville
Florida
Orlando Health
Orlando
Florida
Cleveland Clinic Florida
Weston
Florida
Augusta University
Augusta
Georgia
Northeast Georgia Medical Center
Gainesville
Georgia
WellStar Kennestone Hospital
Marietta
Georgia
Rush University Medical Center
Chicago
Illinois
Prairie Education and Research Cooperative
Springfield
Illinois
HCA Midwest Division, Menorah Medical Center
Overland Park
Kansas
University of Kentucky
Lexington
Kentucky
Baptist Hospital East
Louisville
Kentucky
Ochsner Medical Center
New Orleans
Louisiana
Johns Hopkins University Hospital
Baltimore
Maryland
Tufts Medical Center
Boston
Massachusetts
Charlton Memorial Hospital
Fall River
Massachusetts
McLaren Health Care Corporation
Auburn Hills
Michigan
Henry Ford Hospital
Detroit
Michigan
Children's Hospital of Michigan
Detroit
Michigan
+ 48 more sites — see the full list on the official registry below.
Official registry record
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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