B18.2 I50
Conditions
Interventions
Group 1: Patients are enrolled into the trial, if they are virologically tested positive for HCV. Before the start of therapy we take blood samples and perform an echocardiography.
The treatment with
Sponsors
Klinikum Coburg - REGIOMED
Eligibility
Sex/Gender
All
Age
18 Years to 80 Years
Inclusion criteria
Inclusion criteria: HCV positive patients
Exclusion criteria
Exclusion criteria: HBsAg +, clinically manifested coronary heart disease
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| NT-proBNP: before (initial value) and at the end of therapy (follow up - 12 weeks) | — |
Secondary
| Measure | Time frame |
|---|---|
| echocardiographic measurements (ejection fraction, LVESV, E/A ratio, ..); laboratory measurements: inflammatory markers (CRP, IL6), transaminases (ALT, AST), gGT, AP | — |
Countries
Germany
Contacts
Public ContactDirk Mayer
Klinikum Coburg - REGIOMED
Outcome results
None listed