Cardiac amyloidosis E85.9
Conditions
Interventions
Group 1: Patients with cardiac amyloidosis (all comer registry).
In this observational clinical trial, we aim to study patients with cardiac amyloidosis at disease onset and longitudinal progression t
Sponsors
Deutsches Herzzentrum München, Klinik für Herz- und Kreislauferkrankungen
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: - signed informed consent form - invasively or non-invasively confirmed cardiac amyloidosis
Exclusion criteria
Exclusion criteria: None
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Cardiac decompensation and death one year after initial diagnosis | — |
Secondary
| Measure | Time frame |
|---|---|
| - Baseline clinical, laboratory, echocardiographic, spiroergometric, and functional characteristics. - Change in baseline characteristics during follow-up with symptomatic and/or specific therapy - Serious adverse cardiovascular and cerebrovascular events (MACCE). | — |
Countries
Germany
Contacts
Public ContactPatrick Fuchs
Deutsches Herzzentrum München, Klinik für Herz- und Kreislauferkrankungen
Outcome results
None listed