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
Locations
1Sponsors and collaborators
Marianna Adamo
Lead sponsor
Azienda Socio Sanitaria Territoriale degli Spedali Civili di Brescia
Sponsor institution
San Raffaele University Hospital, Italy
Collaborator