Is NCT06137807 recruiting in Delray Beach, FL?

Yes, NCT06137807 is currently recruiting participants at its Delray Beach, FL location. This tricuspid regurgitation clinical trial is actively enrolling qualified participants.

How do I join the tricuspid regurgitation clinical trial in Delray Beach?

To join this clinical trial in Delray Beach, complete the eligibility form on this page. A study coordinator will contact you to discuss next steps and determine if you qualify.

Is participation in this Delray Beach clinical trial free?

Yes, all study-related care is provided at no cost to qualified participants. Many studies also offer compensation for time and travel expenses.

Tricuspid Regurgitation Clinical Trial in Delray Beach, FL

About This Tricuspid Regurgitation Study in Delray Beach

The TricValve® Transcatheter Bicaval Valve System is a bicaval transcatheter tricuspid valve replacement system, which includes the TricValve® Transcatheter Bicaval Valve for superior vena cava (SVC) and the TricValve® Transcatheter Bicaval Valve for inferior vena cava (IVC). The TricValve® Transcatheter Bicaval Valves are pre-mounted into the TricValve® Delivery System which is used for percutaneous access and delivery of the TricValve® Transcatheter Bicaval Valve in the vena cava. The system is a single use, sterile device compatible with all the valve sizes. The prostheses are implanted percutaneously into the inferior and superior vena cava without disturbing the native tricuspid valve. The device is made of bovine pericardium leaflets sutured on a nitinol self-expanding stent system.

Sponsor: P+F Products + Features USA Inc.

Who Can Participate

Inclusion Criteria

Subject must be 18 years or older, at the time of signing the informed consent.

Subjects has severe tricuspid regurgitation (TR), as determined by the qualifying transthoracic echocardiogram (TTE) confirmed by an echocardiography Core Lab.

NYHA Class III-IVa (not on inotropes, IABP or LVAD) or heart failure (HF) admission in the past 6 months.

Subject is adequately treated with optimal medical therapy (OMT) for heart failure per the local Heart Team for at least 30 days prior to the index procedure, including a diuretic.

The local Heart Team and IEC determine that the patient is eligible for the TricValve procedure.

For females of childbearing potential, negative pregnancy test.

Capable of giving signed informed consent.

Exclusion Criteria

Subject had a recent MI, stroke or cardiovascular accident; underwent coronary artery bypass graft surgery, had a percutaneous coronary intervention or other major cardiovascular surgery within 90 days prior to TricValve implantation.

Subject requires another planned major cardiac procedure, including left-sided transcatheter intervention or surgery (e.g. severe aortic stenosis, severe mitral regurgitation), coronary artery bypass or PCI or pulmonary valve correction. Please note that if closure of an ASD, iatrogenic ASD or PFO is performed, TricValve implantation can be performed 30 days after the intervention. Additionally, TricValve implantation can be performed 30 days after any Electrophysiology procedure (pacemaker, ICD, etc.).

LVEF ≤ 30% on echocardiography.

Evidence of intracardiac, inferior vena cava (IVC), or femoral venous mass, thrombus or vegetation.

Tricuspid stenosis. (Per TVARC, echo criteria: TVA at least 1.5 cm2 or TVAi at least 0.9 cm2/m2 \[at least 0.75 if BMI \>30 kg/m2\], DVI \<2.2, mean gradient \<5mm Hg); reduction of total tricuspid regurgitation to optimal (≤ mild \[1+\]) or acceptable (≤ moderate \[2+\]).

Severe right ventricular dysfunction.

Cardiac amyloidosis

Pulmonary artery systolic pressure (PASP) \>65 mmHg assessed with Echo Doppler and /or right heart catheterization.

Lower extremity venous thrombosis and/or the presence of an IVC filter at the time of or 6 months prior to TricValve procedure.

Hemodynamically significant pericardial effusion.

Patient with refractory heart failure requiring advanced intervention (i.e. left ventricular assist device, transplantation) (ACC/ AHA/ ESC/ EACTS Stage D heart failure)

Any known allergy or hypersensitivity to nitinol, bovine tissue or contrast media that cannot be adequately treated with pre-medication.

Unable to tolerate anticoagulation/antiplatelet therapy

Hemodynamic instability, cardiogenic shock, inotropic support, intra-aortic balloon pump or acute heart failure within 30 days prior to the TricValve procedure.

Any known life-threatening condition with an estimated life span of at least 12 months.

Platelet count \< 75,000/mm3

Child-Pugh Severity Class C (10-15 points).

Severe renal insufficiency with estimated glomerular filtration rate (eGFR) ≤ 25 mL/min/1.73 m2 or requiring chronic renal replacement therapy at the time of enrollment.

Endocarditis or active/ongoing infection requiring antibiotics.

Unable to walk at least 60 meters in a 6minute walk test.

Known bleeding or clotting disorders or patient refuses blood transfusion.

Active gastrointestinal (GI) bleeding within 3 months of randomization.

Presence of significant congenital heart disease including but not limited to hemodynamically significant atrial septal defect, RV dysplasia, and arrhythmogenic RV.

Use or participation in other investigational device or drug study in which patient has not reached a primary endpoint to treat cardiovascular conditions related to the outcomes of the current study.

Any other condition that would preclude ability to meet study requirements in the opinion of the investigator.

Psychiatric/behavioral issues or other medical or social conditions that preclude valid consent and follow-up

Pregnant or breastfeeding subjects and those who plan pregnancy during the clinical investigation follow-up period.

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Delray Beach?

Yes, this clinical trial (NCT06137807) has an active research site in Delray Beach, FL that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Tricuspid Regurgitation Treatment Options in Delray Beach, FL

If you're searching for tricuspid regurgitation treatment options in Delray Beach, FL, this clinical trial (NCT06137807) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Delray Beach research site is actively enrolling participants for this clinical trial. You'll receive care from experienced tricuspid regurgitation specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all tricuspid regurgitation clinical trials near you to find additional studies recruiting in your area.

Tricuspid Regurgitation Clinical Trial in Delray Beach, FL

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