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Encore PFO Closure Device - The PerFOrm Trial

Encore Medical Inc. · with Bright Research Partners, Yale Cardiovascular Research Group · NCT05537753

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Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.

Key facts

Compensation
Not posted. Ask the study team before screening.
Who can join
Ages 18–60 · All sexes
Healthy volunteers
Not accepted (a condition is required)
Study type
Interventional · Not applicable
Target enrollment
500
US sites recruiting
8
Study start
July 12, 2023
Record last updated
September 19, 2024

Status re-checked against ClinicalTrials.gov within the last 12 hours.

What the study is about

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.

Being studied: Encore PFO closure device; FDA-approved PFO closure device

Conditions: Patent Foramen Ovale; Cryptogenic Stroke

Eligibility criteria

Copied from the official record. The study team makes the final decision at screening.

Show full criteria

Inclusion Criteria

  • 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
  • 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

Exclusion Criteria

  • Age \<18 years and age >60 years
  • Greater than 50% lumen diameter stenosis of intracranial or extracranial vessels
  • Intracardiac thrombus or tumor
  • Acute or recent (within 6 months) myocardial infarction (MI) or unstable angina
  • Left ventricular aneurysm or akinesis
  • Mitral valve stenosis (mitral valve area less than 1.5cm2) or severe mitral regurgitation
  • Aortic valve stenosis (gradient >40 mmHg) or severe aortic valve regurgitation
  • Mitral or aortic valve vegetation or prosthesis
  • Left ventricular ejection fraction \<35%
  • 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
  • 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
  • Another source of right-to-left shunts identified at baseline, including an atrial septal defect and/or fenestrated septum
  • Any history of atrial fibrillation/atrial flutter (chronic or intermittent)
  • Active endocarditis or other untreated infections
  • Chronic kidney disease stage 4 or higher or end-stage renal failure requiring dialysis (eGFR less than 30)
  • Severe liver disease (ALT 3X ULN) or documented cirrhosis
  • Lung disease requiring continuous home oxygen
  • Uncontrolled hypertension, defined as sustained elevated blood pressure >160/90 mm Hg on medication
  • Uncontrolled diabetes mellitus, defined as HbA1c greater than 9 (based on most recent test which must have been collected within the last year)
  • Anatomical or physiological structures that do not permit TEE
  • Anticipated need for treatment of structural cardiac defects other than PFO
  • Concomitant cardiac anomalies requiring an operative procedure
  • Hemorrhagic diseases (e.g., coagulopathy, tendency to hemolysis)
  • Hypersensitivity to contrast medium or nickel
  • Contraindication to aspirin or clopidogrel
  • The required sheaths cannot be passed through the relevant vessels for access to the PFO
  • Vulnerable patient (e.g., incarcerated or cognitively challenged adults); see Section 7.2.1
  • Subject is unable or unwilling to provide informed consent
  • Subject is unable to comply with the protocol
  • Any other clinical reasons for which the patient would not be an appropriate candidate for the study, as determined by the site investigators

Recruiting US locations

  • Arkansas Cardiology

    Little Rock, AR 72205

    Site contact: Bobbi Phillips · bphillips@arcard.org

  • Southern CA Permanente Medical Group - Kaiser San Diego and Scripps Memorial Hospital

    La Jolla, CA 92037

    Site contact: Sharon Weaver · 858-824-8261 · Weaver.Sharon@scrippshealth.org

  • University of South Florida

    Tampa, FL 33606

    Site contact: Osama Abou Saleh, MD · 813-259-8835 · oabousaleh@usf.edu

  • Mercy One Iowa Heart Center

    West Des Moines, IA 50266

    Site contact: Jennifer Young, RN · jyoung@iowaheart.com

  • Kansas University Medical Center

    Kansas City, KS 66160

    Site contact: Tilitha Shawgo, RN · 913-588-9720 · tshawgo@kumc.edu

  • Jackson Heart Clinic

    Jackson, MS 39216

    Site contact: Jamie Neal · 601-982-7850 · jneal@jacksonheart.com

  • CHI Health

    Omaha, NE 68124

    Site contact: Barb Lapke · 402-343-8511 · barb.lapke@commonspirit.org

  • Medical University of South Carolina Gazes Research Institute

    Charleston, SC 29425

    Site contact: Virginia Theodorof · theodoro@musc.edu

Study contacts (from the official record)

  • Joseph Marino · 651-797-0913 · jmarino@encore-medical.com
  • Hannah Bearinger · hannah.bearinger@brightresearch.com
All neurology studies in Arkansas →
Encore PFO Closure Device - The PerFOrm Trial (NCT05537753) | Bored Studies