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Tricuspid RegurgitationTRIGISTRYNCT05825898

Outcome of Patients With Severe Functional TR According to Medical, Transcatheter or Surgical Treatment

An observational study of Tricuspid Regurgitation, run by Ottawa Heart Institute Research Corporation at 44 sites in 10 countries.

Enrolling by invitation

Enrolling by invitation. The study team selects and invites participants, usually from an existing group of patients.

Sites and contacts
Official record
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Trial summary

Tricuspid regurgitation (TR) is a public health problem: moderate / severe TR are common, especially in ageing populations, and affect 4% of the population >75 years old, totaling approximately 1.6 million in the US and 3 million in Europe. TR is associated with an increased risk of mortality and morbidity. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Tricuspid Regurgitation
What is being tested?
Surgery or Transcatheter tricuspid valve intervention
Type of treatment
Surgery or procedure
How many people
3,500 participants
Where
44 sitesin 10 countries
Study dates
1 Sep 2022to Dec 2026
Phase
Observational
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: The investigators will enroll 3 populations of patients with isolated functional TR * Patients who remained under conservative management * Patients who underwent an isolated valve surgery * Patients who underwent a transcatheter valve intervention

Who may be able to join

  • Age ≥ 18 years
  • Isolated (no left-valvular heart disease (mitral regurgitation) >2)
  • AND Functional
  • AND Moderate to severe or severe Tricuspid regurgitation

Who cannot join

  • Congenital valvular disease,
  • Previous tricuspid valve intervention,
  • Organic tricuspid valvular disease
  • Associated valvular heart disease

Trial locations and contacts

44 sites in 10 countries. Contact the study team or a site near you to ask about taking part.

44 sites in 10 countries

France12 sites
  • Amiens University Hospital

    Amiens

  • Henri Mondor Hospital

    Créteil

  • CHU Lille

    Lille

  • Department of Cardiovascular Surgery and Transplantation, Louis Pradel Cardiovascular Hospital

    Lyon

  • APHM, La Timone Hospital, Cardiology Department

    Marseille

  • Department of Cardiology, University Hospital of Nancy-Brabois

    Nancy

  • CHU de Nantes

    Nantes

  • Department of Cardiology, Bichat Claude Bernard Hospital

    Paris

  • CHU de RENNES

    Rennes

  • CHU Charles Nicolle

    Rouen

  • Cardiology Department, Centre Cardiologique du Nord

    Saint-Denis

  • Rangueil University Hospital

    Toulouse

Other trials in France

Germany11 sites
  • Herz- und Diabeteszentrum

    Bad Oeynhausen

  • Charité Universitätsmedizin Berlin

    Berlin

  • Bonn University Hospital

    Bonn

  • University of Cologne

    Cologne

  • Cardiovascular center Frankfurt

    Frankfurt

  • Albertinen Heart and Vascular Center

    Hamburg

  • Asklepios clinic Sankt Georg

    Hamburg

  • University Heart and Vascular Center

    Hamburg

  • Leipzig University Hospital

    Leipzig

  • University Medical Center of Mainz

    Mainz

  • Munich Großhadern

    Munich

Other trials in Germany

Spain5 sites
  • Hospital 12 de Octubre

    Madrid

  • Hospital Clínico San Carlos

    Madrid

  • Hospital Gregorio Marañón

    Madrid

  • Hospital Ramón y Cajal

    Madrid

  • Puerta de Hierro

    Madrid

Other trials in Spain

United States4 sites
  • Mount Sinai

    New York, New York, 10029

  • Columbia University Medical Center

    New York, New York, 10032

  • Montefiore Health System

    New York, New York, 10467

  • Mayo Clinic Rochester

    Rochester, Minnesota, 55905

Other trials in United States

Canada4 sites
  • University of Ottawa Heart Institute

    Ottawa, Ontario, K1Y 4W7

  • IUCPQ

    Québec

  • St Michael's Hospital

    Toronto

  • St Paul Hospital

    Vancouver

Other trials in Canada

Switzerland3 sites
  • Hopital Universitaire de Bern

    Bern

  • Istituto Cardiocentro Ticino

    Lugano

  • Zurich Heart Center

    Zurich

Other trials in Switzerland

Italy2 sites
  • Instituto Auxologico Italiano, IRCCS

    Milan

  • San Raffaele University Hospital

    Milan

Other trials in Italy

Austria1 site
  • Vienna Medical University

    Vienna

Other trials in Austria

Israel1 site
  • Tel Aviv Medical center

    Tel Aviv

Other trials in Israel

Netherlands1 site
  • Leiden University Medical center

    Leiden

Other trials in Netherlands

About this study

Official title: Outcome of Patients With Severe Functional Tricuspid Regurgitation

Tricuspid regurgitation (TR) is a public health problem: moderate / severe TR are common, especially in ageing populations, and affect 4% of the population >75 years old, totaling approximately 1.6 million in the US and 3 million in Europe. TR is associated with an increased risk of mortality and morbidity. Contrasting with TR prevalence and the magnitude of the problem, the vast majority of patients are medically treated with diuretics to relieve their symptoms and a curative surgical treatment for isolated severe TR is seldom performed. Reluctance to perform an ITVS can be explained in the one hand by the limited evidence that TR correction improves outcomes and on the other hand, ITVS is associated to high observed in-hospital mortality rates (≈ 10% remarkably consistent in most series across the literature). Severity of the clinical presentation is the main predictor of outcome after surgery. The TRI-SCORE, is a dedicated, simple and accurate risk score model to predict in-hospital mortality after ITVS that could guide the clinical decision-making process at the individual level. Excellent outcomes can be achieved when patients present with low TRI-SCORE. These results suggest adopting a more pro-active approach for TV interventions, and to intervene earlier in the course of the disease in patients with severe isolated TR, irrespective of TR mechanism / etiology, before the occurrence of advanced / irreversible consequences such as severe RV dilatation / dysfunction, renal and liver failure, and intractable heart failure. Recently transcatheter tricuspid valve interventions (TTVI) have emerged recently as a less invasive option to surgery to cure patients with TR.

What is the best treatment between medical, surgical or transcatheter therapy to consider and the best timing for each patient are not clearly defined. The aim of the study is to compare outcome of patients with significant functional TR according to medical, transcatheter or surgical treatment after matching per TRISCORE.

Read the detailed description

Tricuspid regurgitation (TR) is a public health problem: moderate / severe TR are common, especially in ageing populations, and affect 4% of the population >75 years old, totaling approximately 1.6 million in the US and 3 million in Europe. The literature is consistent showing that TR is a serious condition, associated with morbidity (reduction in exercise capacity, heart failure) and mortality that increase with TR severity.

Current American College of Cardiology (ACC) / American Heart Association (AHA) and European Society of Cardiology (ESC) / European Association of Cardio-Thoracic Surgery guidelines (EACTS) guidelines recommend performing an isolated tricuspid valve surgery (ITVS) in patients with severe secondary (and primary) TR (with or without previous left-sided surgery), who are symptomatic or have right ventricle (RV) dilatation, in the absence of severe RV or left ventricular (LV) dysfunction and severe pulmonary vascular hypertension.

Contrasting with TR prevalence and the magnitude of the problem, the vast majority of patients are medically treated with diuretics to relieve their symptoms and a curative surgical treatment for isolated severe TR is seldom performed ITVS represents only 8% of all tricuspid valve (TV) surgeries and a tricuspid valve intervention is mostly performed at the same time that left-sided heart valve surgery. Thus, only 10% of patients admitted in France with a diagnosis of significant TR are referred for an intervention.

Reluctance to perform an ITVS can be explained in the one hand by the limited evidence that TR correction improves outcomes. Indeed, there is no large randomized multicentric study in the literature to compare medical vs surgical treatment of TR. A recent study did not show difference in long-term survival for patients who undergo surgical intervention compared to medical management alone but this was a non-randomized retrospective single-center study with a small propensity matched sample (62 patients in each group) and matching was performed according to parameters that are not specific to the RV. On the other hand, ITVS is associated to high observed in-hospital mortality rates (≈ 10% remarkably consistent in most series across the literature). In a large French multicentric registry of 466 patients gathering all consecutive patients who underwent a non-congenital ITVS on native valve for severe TR at 12 tertiary centers during a 11-year period (2007-2017), in-hospital mortality was 10% as in other series, but this average rate was hiding important disparities. Mortality rate was indeed markedly variable and was predicted by the severity of the pre-operative clinical, biological and echocardiographic presentation while TR mechanism / etiology had limited impact. As there is no dedicated STS risk score model for ITVS, and the logistic EuroSCORE and the EuroSCORE II were not designed for ITVS, the investigators have developed TRI-SCORE, a dedicated, simple and accurate risk score model to predict in-hospital mortality after ITVS that could guide the clinical decision-making process at the individual level. TRI-SCORE was based on eight clinical (age ≥70 years, NYHA functional class III-IV, right-sided heart failure signs, daily dose of furosemide ≥125 mg), laboratory (glomerular filtration rate <30 ml/min, elevated total bilirubin) and echocardiographic (LV ejection fraction <60%, moderate/severe RV dysfunction) parameters easy to ascertain and capturing the impact of TR on the RV, the liver and the kidneys. This risk score model, on a 0-12 points scale, provided both an excellent discrimination (C-index >0.75) and calibration with a predicted mortality rate ranging from 1% for 0 point to 65% for ≥9 points irrespective of TR mechanism / etiology. Half of patients were referred for an intervention late in the course of the disease with moderately (4-6) or severely elevated (>6) scores, and therefore high mortality rates. In contrast, low in-hospital and 1-year mortality rates (0% to 4%) were achieved in patients with low score (≤3). Our results suggest adopting a more pro-active approach for TV interventions, and to intervene earlier in the course of the disease in patients with severe isolated TR, irrespective of TR mechanism / etiology, before the occurrence of advanced / irreversible consequences such as severe RV dilatation / dysfunction, renal and liver failure, and intractable heart failure.

Transcatheter tricuspid valve interventions (TTVI) are still at an early stage with a large number of percutaneous TV devices currently under development. TTVI are mostly a repair, especially edge-to-edge repair, with promising initial results in the first real world registries with patients at high surgical risk. Therefore, TTVI, as a less-invasive alternative to surgery, may push for an extension of the number of patients treated.

What is the best treatment between medical, surgical or transcatheter therapy to consider and the best timing for each patient are not clearly defined. The aim of the study is to compare outcome of patients with significant functional TR according to medical, transcatheter or surgical treatment after matching per TRISCORE.

Being tested
Surgery or Transcatheter tricuspid valve intervention
Medical subject headings
Tricuspid Valve Insufficiency

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Surgery or Transcatheter tricuspid valve interventionProcedure or surgery

    Isolated tricuspid valve surgery or Transcatheter tricuspid valve intervention

Study groups in NCT05825898
Study groupRoleWhat they receive
Conservative managementPatients with TR who did not undergo a tricuspid valve intervention
Receives: Procedure: Surgery or Transcatheter tricuspid valve intervention
Isolated tricuspid valve surgeryPatients with TR who underwent a Isolated tricuspid valve surgery.
Receives: Procedure: Surgery or Transcatheter tricuspid valve intervention
Transcatheter tricuspid valve interventionPatients with TR who underwent a transcatheter tricuspid valve intervention.
Receives: Procedure: Surgery or Transcatheter tricuspid valve intervention

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Survival at 2 years

    Mortality

    Measured: 2 years

Secondary outcomes (2)
  1. Survival free of heart failure admission at 2 years

    Patients alive and never admitted for heart failure

    Measured: 2 years

  2. Survival and heart failure readmissions

    Patients alive or never admitted for heart failure

    Measured: up to 10 years

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted24 Apr 2023
  2. Study start1 Sep 2022
  3. Primary completionDec 2026 (estimated)
  4. Study completionDec 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Case only
Time perspective
Retrospective
Enrolment
3,500 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05825898
Sponsor's protocol ID
TRIGISTRY
Acronym
TRIGISTRY
Status last verified
Apr 2026
First submitted
11 Apr 2023
Last updated
8 May 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: A steering committee will organize the publication plan

Questions about this trial

What is this clinical trial studying?

An observational study of Tricuspid Regurgitation, run by Ottawa Heart Institute Research Corporation at 44 sites in 10 countries.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: enrolling by invitation, as of the sponsor's last update on 8 May 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 44 sites in France, Germany, Spain, United States, Canada and 5 more countries. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Survival at 2 years (time frame: 2 years). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 8 May 2026.

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