tricuspid regurgitation, tricuspid stenosis, pulmonary regurgitation, pulmonary stenosis I36.9
Conditions
Interventions
Group 1: valve interventions of the right heart (tricuspid regurgitation/ stenosis, pulmonary regurgiatation/ stenosis) (planned interventions have a CE Certification and are already established
the aim of the study is to monitor the post-interventional course)
Sponsors
Charité Campus Charité Mitte
Eligibility
Sex/Gender
All
Age
18 Years to 120 Years
Inclusion criteria
Inclusion criteria: Patients with planned or after interventional therapy of tricuspid regurgitation or stenosis or pulmonary regurgitation or stenosis, >18 years, written informed consent
Exclusion criteria
Exclusion criteria: Patients in care or unable to consent; Patients who are unable to comply with follow-up examinations; Patients who are detained in an institution
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Overall mortality, cardiovascular mortality, heart failure hospitalization 2 months after intervention (questionaires). | — |
Secondary
| Measure | Time frame |
|---|---|
| NYHA class, NTproBNP, liver and kidney function (laboratory measurements), valve function, cardiac function, and cardiac morphology 2 months afer intervention. Assessment of parameters with questionnaires, laboratory meassurements and echocardiography. | — |
Countries
Germany
Contacts
Public ContactHenryk Dreger
Deutsches Herzzentrum der Charité (DHZC)
Outcome results
None listed