800 Participants NeededMy employer runs this trial

Transcatheter Valve Replacement for Tricuspid Regurgitation

(TRIPLACE Trial)

Recruiting at 34 trial locations
AS
RP
Overseen ByRishi Puri, MD
Age: 18+
Sex: Any
Trial Phase: Academic
Sponsor: Montefiore Medical Center
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial aims to understand the safety and effectiveness of transcatheter tricuspid valve replacement (TTVR) for individuals with tricuspid regurgitation, a condition where the heart’s tricuspid valve doesn't close tightly, causing blood to flow backward. Researchers seek to identify which patients might face complications, such as needing a pacemaker, and how to best manage these situations. This trial is for those diagnosed with significant tricuspid valve issues who require the TTVR procedure. As a Phase 3 trial, it represents the final step before FDA approval, offering participants the opportunity to contribute to a potentially groundbreaking treatment.

Do I need to stop my current medications for the trial?

The trial information does not specify whether you need to stop taking your current medications. It's best to discuss this with the trial coordinators or your doctor.

What prior data suggests that transcatheter tricuspid valve replacement is safe?

Research has shown that Transcatheter Tricuspid Valve Replacement (TTVR) is generally well-tolerated by patients. One study found that TTVR was successfully performed in 94% of cases. The in-hospital death rate was low at 1.37%, and the 30-day death rate was only 2.49%. Serious issues were rare, with only 1.7% of patients experiencing major problems within the first 30 days. After one year, this rate increased to 12.7%.

These findings suggest that TTVR is relatively safe for patients. While no treatment is without risk, evidence indicates that serious complications are uncommon, especially in the short term.12345

Why are researchers excited about this trial?

Unlike the standard of care for tricuspid regurgitation, which often involves open-heart surgery to repair or replace the valve, transcatheter tricuspid valve replacement (TTVR) is a minimally invasive alternative. Researchers are excited about TTVR because it doesn't require opening the chest, significantly reducing recovery time and risk for patients who might not be candidates for surgery. This approach uses catheters to replace the valve through blood vessels, offering a promising option for patients with severe symptoms who need a less invasive solution.

What evidence suggests that transcatheter tricuspid valve replacement is effective for tricuspid regurgitation?

Studies have shown that Transcatheter Tricuspid Valve Replacement (TTVR), which participants in this trial will undergo, can greatly reduce tricuspid regurgitation, a condition where the heart's tricuspid valve leaks. Research indicates that the procedure succeeds 94% of the time. Patients often experience improved well-being and a higher quality of life after the treatment. Additionally, TTVR is associated with low mortality rates both in the hospital and 30 days post-procedure. Long-term results also demonstrate better survival rates compared to other treatments.12567

Who Is on the Research Team?

AS

Andrea Scotti, MD

Principal Investigator

Montefiore Medical Center

AL

Azeem Latib, MD

Principal Investigator

Montefiore Medical Center

TM

Thomas Modine, MD

Principal Investigator

University Hospital, Bordeaux

RP

Rishi Puri, MD

Principal Investigator

The Cleveland Clinic

NF

Neil Fam, MD

Principal Investigator

St. Michaels Hospital

Are You a Good Fit for This Trial?

Inclusion Criteria

You have had a tricuspid valve implanted in its normal anatomical position.
You are having a Transcatheter Tricuspid Valve Replacement.
You have a congenital heart condition with Tricuspid Valve disease.

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Treatment

Participants undergo Transcatheter Tricuspid Valve Replacement (TTVR)

1 day
1 visit (in-person)

Follow-up

Participants are monitored for safety and effectiveness after TTVR, including assessment of procedural and device-related complications

30 days
Multiple visits (in-person and virtual)

Long-term Follow-up

Participants are monitored for long-term outcomes, including tricuspid valve reintervention and quality of life assessments

12 months
Periodic visits (in-person and virtual)

What Are the Treatments Tested in This Trial?

Interventions

  • Transcatheter Tricuspid Valve Replacement

How Is the Trial Designed?

1

Treatment groups

Experimental Treatment

Group I: Patients with Tricuspid Regurgitation undergoing Transcatheter Tricuspid Valve ReplacementExperimental Treatment1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Montefiore Medical Center

Lead Sponsor

Trials
468
Recruited
599,000+

University of Toronto

Collaborator

Trials
739
Recruited
1,125,000+

University Hospital, Bordeaux

Collaborator

Trials
813
Recruited
825,000+

The Cleveland Clinic

Collaborator

Trials
1,072
Recruited
1,377,000+

Citations

Clinical Outcomes Following Transcatheter Tricuspid Valve ...

TTVR was associated with low in-hospital (1.37%) and 30-day (2.49%) mortality rates, with significant reduction in tricuspid regurgitation and improvement in ...

Efficacy and Safety of Transcatheter Tricuspid Valve ...

Twenty‐one studies with 643 patients (mean age 75.8 years, 70.76% female) reported a 94% technical success rate for TTVR (95% CI: 91–96%). 30‐ ...

1-Year Results From TRISCEND II Pivotal Trial

Treatment of patients with symptomatic and severe or greater TR with TTVR+OMT resulted in substantial improvement in patients' symptoms, function, and quality ...

Comparing outcomes of transcatheter tricuspid valve ...

The TTVR group had better 2-years survival (75.8% and 48.4%, P = 0.019) and freedom from 2-years combined endpoint (61.5% vs 45.9%, P = 0.007) ...

Transcatheter Repair for Patients with Tricuspid ...

TEER was found to be safe; 98.3% of the patients who underwent the procedure were free from major adverse events at 30 days. Conclusions.

Transcatheter valve repair of tricuspid regurgitation: 1-year ...

Tricuspid regurgitation was reduced to ≤moderate in 87.7% of patients (p<0.001). The composite MAE rate was 1.7% at 30 days and 12.7% at 1 year.

Early Outcomes of Real-World Transcatheter Tricuspid ...

The aim of this study was to investigate the real-world safety and efficacy of the EVOQUE TTVR system in patients with severe TR treated at 12 experienced heart ...