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Edwards PASCAL Transcatheter Valve Repair System Pivotal Clinical Trial
Not Recruiting
Trial ID: NCT04097145
Purpose
To establish the safety and effectiveness of the Edwards PASCAL Transcatheter Repair System
in patients with symptomatic severe tricuspid regurgitation who have been determined to be at
an intermediate or greater estimated risk of mortality with tricuspid valve surgery by the
cardiac surgeon with concurrence by the local Heart Team
Official Title
A Prospective, Multicenter, Randomized, Controlled Pivotal Trial to Evaluate the Safety and Effectiveness of Transcatheter Tricuspid Valve Repair With the Edwards PASCAL Transcatheter Valve Repair System and Optimal Medical Therapy (OMT) Compared to OMT Alone in Patients With Tricuspid Regurgitation
Stanford Investigator(s)
Jack Boyd
Clinical Associate Professor, Cardiothoracic Surgery
Mirela Tuzovic
Clinical Assistant Professor, Medicine - Cardiovascular Medicine
Rahul P Sharma, MBBS, FRACP
Clinical Associate Professor, Medicine - Cardiovascular Medicine
Randall Vagelos, MD
Professor of Medicine (Cardiovascular)
David Lee, MD
Professor of Medicine (Cardiovascular Medicine)
Eligibility
Inclusion Criteria:
- Eighteen (18) years of age or older
- Despite medical therapy, per the local Heart Team, patient has signs of TR, symptoms
from TR, or prior heart failure hospitalization from TR.
- Severe or greater tricuspid regurgitation
- New York Heart Association (NYHA) Class II-IVa or heart failure hospitalization in the
prior 12 months
- Patient is at an intermediate or greater estimated risk of mortality with tricuspid
valve surgery as determined by the cardiac surgeon with concurrence by the local Heart
Team
- Patient is able and willing to give informed consent, follow protocol procedures, and
comply with follow-up visit requirements
Exclusion Criteria:
- Tricuspid valve anatomy not evaluable by TTE or TEE
- Tricuspid valve anatomy precludes proper device deployment and function
- Patient with refractory heart failure requiring, advanced intervention (i.e. patient
has or will need left ventricular assist device, or transplantation) (ACC/AHA Stage D
heart failure)
- Presence of trans-tricuspid pacemaker or defibrillator leads which meet one of the
following:
1. Would prevent proper TR reduction due to interaction of the lead with the
leaflets
2. Were implanted in the RV within the last 90 days prior to the point of enrollment
- Primary non-degenerative tricuspid disease
- Previous tricuspid valve repair or replacement that would interfere with placement of
PASCAL
- Clinically significant, untreated coronary artery disease requiring revascularization,
unstable angina, evidence of acute coronary syndrome, recent myocardial infarction
- Significant intra-cardiac mass, thrombus, or vegetation per echo core lab assessment
- Deep vein thrombosis (DVT) or pulmonary embolism (PE) in the last 90 days
- Recent Stroke
- Active gastrointestinal (GI) bleeding
- Presence of infiltrative cardiomyopathy or valvulopathy (including carcinoid,
amyloidosis, sarcoidosis, hemochromatosis) or significant congenital heart disease,
including but not limited to atrial septal defect, RV dysplasia, and arrhythmogenic RV
- Need for emergent or urgent surgery for any reason, any planned cardiac surgery within
the next 12 months (365 days), or any planned percutaneous cardiac procedure within
the next 90 days
- Any of the following cardiovascular procedures:
1. Percutaneous coronary, intracardiac, or endovascular intervention within the last
30 days prior to the point of enrollment
2. Carotid surgery within 30 days prior to the point of enrollment
3. Direct current cardioversion within the last 30 days prior to the point of
enrollment
4. Leadless RV pacemaker implant within the last 30 days prior to the point of
enrollment
5. Cardiac surgery within 90 days prior to the point of enrollment
- Severe aortic, mitral and/or pulmonic valve stenosis and/or regurgitation
- Known history of untreated severe symptomatic carotid stenosis or asymptomatic carotid
stenosis
- Active endocarditis within the last 90 days or infection requiring antibiotic therapy
within the last 14 days
- Patient is oxygen-dependent or requires continuous home oxygen
- Pregnant, breastfeeding, or planning pregnancy within the next 12 months (365 days)
- Concurrent medical condition with a life expectancy of less than 12 months in the
judgment of the Investigator
- Patient is currently participating in another investigational biologic, drug, or
device clinical study
- Patient has other medical, social, or psychological conditions that preclude
appropriate consent and follow-up, or the patient is under guardianship
- Any patient considered to be vulnerable
Intervention(s):
device: Edwards PASCAL System
drug: Optimal Medical Therapy
Not Recruiting
Contact Information
Stanford University
School of Medicine
300 Pasteur Drive
Stanford,
CA
94305