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

Conditions

Eligibility

Eligible Ages
Over 18 Years
Eligible Genders
All
Accepts Healthy Volunteers
No

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

Study Design

Phase
N/A
Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel Assignment
Primary Purpose
Treatment
Masking
None (Open Label)

Arm Groups

ArmDescriptionAssigned Intervention
Experimental
Edwards PASCAL System & OMT
Transcatheter tricuspid valve repair with the Edwards PASCAL system in patients on optimal medical therapy (OMT) with tricuspid regurgitation
  • Device: Edwards PASCAL System
    Transcatheter tricuspid valve repair with the Edwards PASCAL System in patients on optimal medical therapy
    Other names:
    • Transcatheter tricuspid valve repair (TTVr)
Active Comparator
Optimal Medical Therapy (OMT)
Optimal medical therapy (OMT) alone in patients with tricuspid regurgitation
  • Drug: Optimal Medical Therapy
    Optimal Medical Therapy alone in patients with tricuspid regurgitation
Experimental
Single-Arm Registry
Transcatheter tricuspid valve repair with the Edwards PASCAL System in conjunction with optimal medical therapy (OMT) in patients with tricuspid regurgitation who are not eligible for randomization
  • Device: Edwards PASCAL System
    Transcatheter tricuspid valve repair with the Edwards PASCAL System in conjunction with OMT

Recruiting Locations

Banner University Medical Center Phoenix
Phoenix, Arizona 85006

More Details

Status
Recruiting
Sponsor
Edwards Lifesciences

Study Contact

Edwards TMTT Clinical Affairs
(949) 250-2500
TMTT_Clinical@edwards.com

Detailed Description

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. Patients will be seen for follow-up visits at discharge, 30 days, 3 months, 6 months, and annually through 5 years.

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.