Encore PFO Closure Device - The PerFOrm Trial
Encore Medical Inc. · with Bright Research Partners, Yale Cardiovascular Research Group · NCT05537753
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
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