I50.9
Conditions
Interventions
Group 1: Women with early breast cancer scheduled for chemotherapy that include therapy regimes with cardiotoxic potential.
Sponsors
Universitätsklinikum Freiburg - Universitäts-Herzzentrum Freiburg-Bad Krozingen
Eligibility
Sex/Gender
Female
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Informed consent Age =18 years Women with early breast cancer scheduled for chemotherapy that include cardiotoxic agents
Exclusion criteria
Exclusion criteria: Severe renal insufficiency (GFR2xULN (250 pg/ml) life expectancy of =12 weeks
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Reduction of the LV-EF (10 absolute point reduction or below 50%) or the global longitudinal strain by 10% or death in the first 12 months | — |
Secondary
| Measure | Time frame |
|---|---|
| Elevation of cardiac biomarkers (NT-proBNP, high sensitive TroponinT) Change of natriuretic peptides and/or cGMP levels Change of other biomarker levels Clinical symptoms of heart failure (NYHA classification) Occurrence of diastolic heart failure Occurrence of ventricular or supraventricular arrhythmias | — |
Countries
Germany
Contacts
Public ContactIstvan Bojti
Universitätsklinikum Freiburg - Universitäts-Herzzentrum Freiburg-Bad Krozingen
Outcome results
None listed