Encore PFO Closure Device - The PerFOrm Trial

Description

The objective of this study is to establish reasonable assurance of safety, effectiveness, and noninferiority of the Encore PFO closure device when compared to any investigator chosen FDA-approved PFO closure device.

Conditions

Patent Foramen Ovale, Cryptogenic Stroke

Study Overview

Study Details

Study overview

The objective of this study is to establish reasonable assurance of safety, effectiveness, and noninferiority of the Encore PFO closure device when compared to any investigator chosen FDA-approved PFO closure device.

Encore PFO Closure Device U.S. IDE Randomized Trial - The PerFOrm Trial

Encore PFO Closure Device - The PerFOrm Trial

Condition
Patent Foramen Ovale
Intervention / Treatment

-

Contacts and Locations

Little Rock

Arkansas Cardiology, Little Rock, Arkansas, United States, 72205

La Jolla

Southern CA Permanente Medical Group - Kaiser San Diego and Scripps Memorial Hospital, La Jolla, California, United States, 92037

Tampa

University of South Florida, Tampa, Florida, United States, 33606

West Des Moines

Mercy One Iowa Heart Center, West Des Moines, Iowa, United States, 50266

Kansas City

Kansas University Medical Center, Kansas City, Kansas, United States, 66160

Jackson

Jackson Heart Clinic, Jackson, Mississippi, United States, 39216

Omaha

CHI Health, Omaha, Nebraska, United States, 68124

Charleston

Medical University of South Carolina Gazes Research Institute, Charleston, South Carolina, United States, 29425

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • 1. Diagnosis of PFO, defined as visualization of microbubbles per TEE in the left atrium within three cardiac cycles from the right atrial opacification demonstrating right-to-left shunting at rest and/or during Valsalva release
  • 2. Cryptogenic stroke within the last 270 days; stroke is defined as acute focal neurological deficit, presumed to be due to focal ischemia, and confirmed by MRI or CT to be a new, neuroanatomically relevant cerebral infarct
  • 1. Age \<18 years and age \>60 years
  • 2. Greater than 50% lumen diameter stenosis of intracranial or extracranial vessels
  • 3. Intracardiac thrombus or tumor
  • 4. Acute or recent (within 6 months) myocardial infarction (MI) or unstable angina
  • 5. Left ventricular aneurysm or akinesis
  • 6. Mitral valve stenosis (mitral valve area less than 1.5cm2) or severe mitral regurgitation
  • 7. Aortic valve stenosis (gradient \>40 mmHg) or severe aortic valve regurgitation
  • 8. Mitral or aortic valve vegetation or prosthesis
  • 9. Left ventricular ejection fraction \<35%
  • 10. Other identifiable cause of stroke, including but not limited to aortic arch plaques (protruding \>4 mm into the lumen), large artery atherosclerotic disease, an established cardioembolic source, small-vessel occlusive disease, or arterial dissection
  • 11. Evidence of a hypercoagulable disorder requiring anticoagulation therapy; this determination will be based on the evaluation of: anticardiolipin antibody (Ab) of the IgG or IgM type, Lupus anticoagulant, B2-glycoprotein-1 Ab, and fasting plasma homocysteine
  • 12. Another source of right-to-left shunts identified at baseline, including an atrial septal defect and/or fenestrated septum
  • 13. Any history of atrial fibrillation/atrial flutter (chronic or intermittent)
  • 14. Active endocarditis or other untreated infections
  • 15. Chronic kidney disease stage 4 or higher or end-stage renal failure requiring dialysis (eGFR less than 30)
  • 16. Severe liver disease (ALT 3X ULN) or documented cirrhosis
  • 17. Lung disease requiring continuous home oxygen
  • 18. Uncontrolled hypertension, defined as sustained elevated blood pressure \>160/90 mm Hg on medication
  • 19. Uncontrolled diabetes mellitus, defined as HbA1c greater than 9 (based on most recent test which must have been collected within the last year)
  • 20. Anatomical or physiological structures that do not permit TEE
  • 21. Anticipated need for treatment of structural cardiac defects other than PFO
  • 22. Concomitant cardiac anomalies requiring an operative procedure
  • 23. Hemorrhagic diseases (e.g., coagulopathy, tendency to hemolysis)
  • 24. Hypersensitivity to contrast medium or nickel
  • 25. Contraindication to aspirin or clopidogrel
  • 26. The required sheaths cannot be passed through the relevant vessels for access to the PFO
  • 27. Vulnerable patient (e.g., incarcerated or cognitively challenged adults); see Section 7.2.1
  • 28. Subject is unable or unwilling to provide informed consent
  • 29. Subject is unable to comply with the protocol
  • 30. Any other clinical reasons for which the patient would not be an appropriate candidate for the study, as determined by the site investigators

Ages Eligible for Study

18 Years to 60 Years

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Encore Medical Inc.,

Christopher D Nielsen, MD, PRINCIPAL_INVESTIGATOR, Medical University of South Carolina

Study Record Dates

2030-10