NCT04634266Active, not recruiting
TRICuspid Intervention in Heart Failure Trial
TRICuspid Intervention in Heart Failure Trial (TRICI-HF-DZHK24)
Source: ClinicalTrials.gov · Last updated 22 May 2026
Brief summary (registry, in English)
Aims: Tricuspid regurgitation (TR) is a detrimental disease frequently diagnosed in patients with right-sided heart failure (HF). While transcatheter tricuspid valve interventions (TTVI) effectively reduce TR and improve quality of life (QoL) in earlier stages of the disease, their effect on reducing HF hospitalizations (HFH) and improving survival remains unclear. Methods: TRIC-I-HF-DZHK24 is an investigator-initiated, prospective, randomized, open-label, multi-center strategy trial. Approximately 360 patients with severe TR and manifest right-sided HF will be enrolled. In contrast to previous trials, subjects with increased risk for HFH will be selected as facilitated by specific inclusion criteria: HFH in the previous year, or presence of cardio-renal syndrome, or evidence for cardio-hepatic syndrome. Subjects will be randomized 2:1 to TTVI and optimal medical therapy (OMT) or continuation of OMT alone. All CE-marked transcatheter repair devices including tricuspid transcatheter edge-to-edge repair (T-TEER) or transcatheter tricuspid annuloplasty can be used for TTVI. The participating 29 study sites are highly experienced in T-TEER. The primary outcome will be assessed at one year. First, a composite of all-cause mortality, HFH, and QoL improvement will be tested hierarchically. If positive, the combination of hard clinical endpoints including all-cause mortality and HFH will be tested. Patients will be followed for a total of 3 years. The safety outcome comprises complications of TTVI, life threatening bleeding and death. Conclusions: The TRIC-I-HF-DZHK24 trial will define the role of TTVI in patients with severe TR and right-sided HF.
- Status (registry)
- Active, not recruiting
- Study type
- Interventional
- Enrollment
- 360 (estimated)
- First submitted
- 17 Nov 2020
- Start date
- 25 Mar 2022
- Primary completion date
- 1 Jul 2026
- Lead sponsor
- LMU Klinikum
- Diseases
- Heart failure
- NCT number
- NCT04634266
What you commit to
- Study type: Interventional
- Planned participants: 360
- From 25 Mar 2022 to the primary completion date, 1 Jul 2026
- 28 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Criteria the registry did not label
- The following inclusion criteria were defined to assure generalizability of the population to be studied:
- Subject is symptomatic due to severe TR despite being on stable OMT for at least 30 days based on judgment of the local heart team.
- Subject is at intermediate or greater estimated risk of morbidity and mortality, defined as a) hospitalization for heart failure during the previous 12 months, or b) cardio-renal syndromea or c) cardio-hepatic syndrome
- New York Heart Association (NYHA) Functional Class II, III or IVa
- Femoral vein access and valve anatomy are determined to be feasible for interventional treatment (including sufficient quality of TTE and TEE imaging)
- Age ≥ 18 years at time of consent
- Subject must provide written informed consent prior to any trial related procedure
- The following exclusion criteria were selected to define a representative study cohort:
- Presence of severe aortic, mitral or pulmonary valve disease OR surgical/interventional treatment at the aortic, mitral or pulmonary valves prior 60 days
- Right heart catheterization (mandatory) with systolic pulmonary artery pressure \> 70 mmHg or substantial pre-capillary pulmonary hypertension (defined as mean pulmonary artery pressure (mPAP) \>30 mmHg plus transpulmonary gradient (TPG) \>17 mmHg or pulmonary vascular resistance (PVR) \>5 wood units)
- Tricuspid valve stenosis (tricuspid mean gradient \> 5 mmHg)
- Pacemaker or ICD leads that would prevent appropriate TTVT
- Prior tricuspid valve procedures or tricuspid valve leaflet anatomy that would interfere with appropriate TTVT (e.g. calcification, Ebstein anomaly, coaptation defect \> 8mm for planned leaflet- and annuloplasty-based therapy)
- Chronic renal failure requiring dialysis
- Tricuspid valve anatomy not evaluable by TTE and TEE
- Myocardial infarction or cerebrovascular accident within prior 90 days
- Life expectancy of less than 12 months
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (28)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Herz- und Diabeteszentrum Nordrhein-Westfalen Coordinator of this site? Confirm its status | Bad Oeynhausen | Germany | Unknown status |
| Deutsches Herzzentrum Berlin Coordinator of this site? Confirm its status | Berlin | Germany | Unknown status |
| Charité Universitätsmedizin Berlin Coordinator of this site? Confirm its status | Berlin | Germany | Unknown status |
| Immanuel Klinikum Bernau Herzzentrum Brandenburg Coordinator of this site? Confirm its status | Bernau | Germany | Unknown status |
| Universitätsklinikum Bonn Coordinator of this site? Confirm its status | Bonn | Germany | Unknown status |
| Herzzentrum Bremen Coordinator of this site? Confirm its status | Bremen | Germany | Unknown status |
| Herzzentrum Uniklinik Köln Coordinator of this site? Confirm its status | Cologne | Germany | Unknown status |
| St.-Johannes-Hospital Dortmund Coordinator of this site? Confirm its status | Dortmund | Germany | Unknown status |
| Universitätsklinikum Düsseldorf Coordinator of this site? Confirm its status | Düsseldorf | Germany | Unknown status |
| Helios Klinikum Erfurt Coordinator of this site? Confirm its status | Erfurt | Germany | Unknown status |
| Universitätsklinikum Essen Coordinator of this site? Confirm its status | Essen | Germany | Unknown status |
| Universitätsklinikum Frankfurt Coordinator of this site? Confirm its status | Frankfurt | Germany | Unknown status |
| Universitätsklinikum Freiburg Coordinator of this site? Confirm its status | Freiburg im Breisgau | Germany | Unknown status |
| Katholisches Marienkrankenhaus Hamburg Coordinator of this site? Confirm its status | Hamburg | Germany | Unknown status |
| Asklepios Klinikum St. Georg Coordinator of this site? Confirm its status | Hamburg | Germany | Unknown status |
| Herzzentrum UKE Coordinator of this site? Confirm its status | Hamburg | Germany | Unknown status |
| Universitätsklinikum Heidelberg Coordinator of this site? Confirm its status | Heidelberg | Germany | Unknown status |
| Universitätsklinikum Jena Coordinator of this site? Confirm its status | Jena | Germany | Unknown status |
| Universitatsklinikum Schleswig-Holstein Coordinator of this site? Confirm its status | Kiel | Germany | Unknown status |
| Herzentrum Leipzig Coordinator of this site? Confirm its status | Leipzig | Germany | Unknown status |
| Universitätsklinikum Schlewsig-Holstein Campus Lübeck Coordinator of this site? Confirm its status | Lübeck | Germany | Unknown status |
| Universitätsmedizin Mainz Coordinator of this site? Confirm its status | Mainz | Germany | Unknown status |
| LMU Klinikum Coordinator of this site? Confirm its status | München | Germany | Unknown status |
| Herzzentrum Siegburg Coordinator of this site? Confirm its status | Siegburg | Germany | Unknown status |
| Robert Bosch Klinikum Stuttgart Coordinator of this site? Confirm its status | Stuttgart | Germany | Unknown status |
| Universitätsklinikum Tübingen Coordinator of this site? Confirm its status | Tübingen | Germany | Unknown status |
| Universitätsklinikum Ulm Coordinator of this site? Confirm its status | Ulm | Germany | Unknown status |
| HELIOS Klinikum Wuppertal Coordinator of this site? Confirm its status | Wuppertal | Germany | Unknown status |
Related publications
- Tricuspid-Valve Intervention in Heart Failure.N Engl J Med · 2026 · PMID 42670975
This page is information, not medical advice. Discuss any trial with your doctor.