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International Multisite Transcatheter Tricuspid Valve Therapies Registry

International Multisite Transcatheter Tricuspid Valve Therapies Registry

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03416166
Acronym
TriValve
Enrollment
269
Registered
2018-01-30
Start date
2016-11-01
Completion date
2026-11-01
Last updated
2018-01-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Severe Tricuspid Regurgitation

Keywords

Tricuspid Valve, tricuspid regurgitation, transcatheter tricuspid regurgitation

Brief summary

For a long time, tricuspid valve disease has been considered as less important than left-sided valvular heart disease. If treated in an advanced stage and simultaneously with other cardiac diseases, it is associated with significant morbidity and mortality. Hence, physicians tend to refer patients more aggressively to surgery (1). Transcatheter procedures are an attractive alternative in high-risk patients. The field of transcatheter tricuspid devices has rapidly advanced over the last few years (2). Limited knowledge is available regarding the epidemiologic and anatomical settings in which these therapies are preferentially applied. The main purpose of this registry is the collection of baseline clinical and anatomical data of the patients treated with transcatheter tricuspid valve therapies, and their outcomes, whenever feasible. Apart from more knowledge regarding the current status in this field, the results could also help the establishment of guidelines with respect to the choice of the transcatheter device selected and to understand which therapy can provide the better outcome in the different anatomies. Moreover, this study will provide important information about the epidemiology of severe tricuspid regurgitation, which is at the moment an undertreated disease.

Interventions

DEVICETranscatheter Tricuspid Intervention

Any available transcatheter tricuspid valve intervention

Sponsors

University of Zurich
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 99 Years

Inclusion criteria

* All the patients undergoing transcatheter tricuspid valve intervention. General inclusion criteria: * Minimal age: 18 years * Patient is able to give written informed consent to the procedure

Exclusion criteria

* Patients not fulfilling the indications for transcatheter tricuspid intervention

Design outcomes

Primary

MeasureTime frame
Cardiovascular Death30 days

Secondary

MeasureTime frame
NYHA Class30 days, 1 year
TR Reduction30 days, 1 year

Countries

Switzerland

Contacts

Primary ContactMaurizio Taramasso, MD, PhD
maurizio.taramasso@usz.ch0041442553728

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 26, 2026