Recruiting

Encore PFO Closure

Sponsor:

Encore Medical Inc.

Code:

NCT05537753

Conditions

Patent Foramen Ovale

Cryptogenic Stroke

Eligibility Criteria

Sex: All

Age: 18 - 60

Healthy Volunteers: Not accepted

Interventions

Encore PFO closure device

FDA-approved PFO closure device

Study Details

Brief summary:

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 ID

NCT05537753

Start date

Jul 12, 2023

Status verified date

Sep, 2024

Completion date

Oct, 2030

Anticipated

Primary completion date

Apr, 2026

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18 - 60

Healthy Volunteers: Not accepted

Inclusion 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

Exclusion Criteria:

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

Study Design

Enrollment

500 participants

Anticipated

Allocation

Randomized

Intervention Model

Parallel Assignment

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

experimental: Encore PFO closure device

active comparator: Any FDA-approved PFO closure device chosen by the investigator

Interventions

Encore PFO closure device

The Encore PFO closure device comprises an implant component and a single-use delivery system.

FDA-approved PFO closure device

Chosen by the investigator

Primary outcome measure

  • Safety: The incidence of device- or procedure-related serious adverse events (SAEs) [ Time Frame: 6 months ]
  • Effectiveness: Effective closure [ Time Frame: 6 months ]

Central Contacts and Locations

Locations

Arkansas Cardiology

Recruiting

Little Rock, Arkansas, United States, 72205

Contacts

Principal Investigator:

Ernesto Ruiz-Rodriguez, MD

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

Recruiting

La Jolla, California, United States, 92037

Contacts

Principal Investigator:

Jeffrey Cavendish, MD

University of South Florida

Recruiting

Tampa, Florida, United States, 33606

Contacts

Vlastibor Minarovjech

minarovjech@usf.edu

Principal Investigator:

Bibhu Mohanty, MD

Mercy One Iowa Heart Center

Recruiting

West Des Moines, Iowa, United States, 50266

Contacts

Jennifer Young, RN

jyoung@iowaheart.com

Principal Investigator:

Mark Tannenbaum, MD

Kansas University Medical Center

Recruiting

Kansas City, Kansas, United States, 66160

Contacts

Principal Investigator:

Georges Hajj, MD

Jackson Heart Clinic

Recruiting

Jackson, Mississippi, United States, 39216

Contacts

Principal Investigator:

William Crowder, MD

CHI Health

Recruiting

Omaha, Nebraska, United States, 68124

Contacts

Principal Investigator:

Himanshu Agarwal, MD

Medical University of South Carolina Gazes Research Institute

Recruiting

Charleston, South Carolina, United States, 29425

Contacts

Virginia Theodorof

theodoro@musc.edu

Kavin Panneerselvam

panneeer@musc.edu

Principal Investigator:

Christopher D Nielsen, MD

More Information

Sponsor

Encore Medical Inc.

Last update posted

Sep 19, 2024

Last verified

Sep, 2024

Keywords

  • PFO closure
  • Stroke

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by Encore Medical Inc. on 2024-09-19.