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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
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

Full criteria on ClinicalTrials.gov

Sites (28)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Herz- und Diabeteszentrum Nordrhein-Westfalen
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Bad OeynhausenGermanyUnknown status
Deutsches Herzzentrum Berlin
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BerlinGermanyUnknown status
Charité Universitätsmedizin Berlin
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BerlinGermanyUnknown status
Immanuel Klinikum Bernau Herzzentrum Brandenburg
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BernauGermanyUnknown status
Universitätsklinikum Bonn
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BonnGermanyUnknown status
Herzzentrum Bremen
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BremenGermanyUnknown status
Herzzentrum Uniklinik Köln
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CologneGermanyUnknown status
St.-Johannes-Hospital Dortmund
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DortmundGermanyUnknown status
Universitätsklinikum Düsseldorf
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DüsseldorfGermanyUnknown status
Helios Klinikum Erfurt
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ErfurtGermanyUnknown status
Universitätsklinikum Essen
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EssenGermanyUnknown status
Universitätsklinikum Frankfurt
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FrankfurtGermanyUnknown status
Universitätsklinikum Freiburg
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Freiburg im BreisgauGermanyUnknown status
Katholisches Marienkrankenhaus Hamburg
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HamburgGermanyUnknown status
Asklepios Klinikum St. Georg
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HamburgGermanyUnknown status
Herzzentrum UKE
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HamburgGermanyUnknown status
Universitätsklinikum Heidelberg
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HeidelbergGermanyUnknown status
Universitätsklinikum Jena
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JenaGermanyUnknown status
Universitatsklinikum Schleswig-Holstein
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KielGermanyUnknown status
Herzentrum Leipzig
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LeipzigGermanyUnknown status
Universitätsklinikum Schlewsig-Holstein Campus Lübeck
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LübeckGermanyUnknown status
Universitätsmedizin Mainz
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MainzGermanyUnknown status
LMU Klinikum
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MünchenGermanyUnknown status
Herzzentrum Siegburg
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SiegburgGermanyUnknown status
Robert Bosch Klinikum Stuttgart
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StuttgartGermanyUnknown status
Universitätsklinikum Tübingen
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TübingenGermanyUnknown status
Universitätsklinikum Ulm
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UlmGermanyUnknown status
HELIOS Klinikum Wuppertal
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WuppertalGermanyUnknown status

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