About this trial
This is an observational, multi-center, retrospective and prospective study collecting data about patients undergoing transcatheter tricuspid valve interventions in a real world clinical environment. The aim is to report clinical characteristics, procedural results and short- and long-term outcomes of patients undergoing transcatheter tricuspid valve interventions in Italian centres.
Eligibility criteria
Qualifiers
Patients undergoing transcatheter treatment of tricuspid regurgitation (native valve -with or without previous surgical valve repair - or degenerated bioprosthesis)
Patients who are willing and capable of providing informed consent, and participating in all follow-ups associated with this clinical investigation.
Disqualifiers
Valve anatomy unsuitable for transcatheter tricuspid valve interventions.
Subjects who are unable or not willing to complete follow-up visits and examination for the duration of the study.
Trial design
Treatments tested in this trial
- Transcatheter tricuspid valve interventions
Treatment groups
Sponsors and collaborators
Marianna Adamo
Lead sponsor
Azienda Socio Sanitaria Territoriale degli Spedali Civili di Brescia
Sponsor institution
San Raffaele University Hospital, Italy
Collaborator