I42 G71.0
Conditions
Interventions
Group 1: No intervention planned. Patients will be invited to our cardiomyopathy outpatients’ clinic and trial blood samples will be withdrawn. Serial blood sampling at 0 hour and 1 hour and after 6 m
Sponsors
Universitätsklinikum Heidelberg/Innere III - Abteilung für Kardiologie, Angiologie und Pneumologie
Eligibility
Sex/Gender
All
Age
18 Years to 100 Years
Inclusion criteria
Inclusion criteria: - Written informed consent - Diagnosed dystrophic myopathy - Age >18 years
Exclusion criteria
Exclusion criteria: - Patients with poor veins - Chronic hemodialysis - No consent
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Primary goals: - Prevalence of stable troponin cinetics defined as troponin T high sensitive (hour 0) : troponin T high sensitive (hour 1) < 5 ng/l Secondary: - Calculation of the reference change value (RCV) within 6 months follow-up (5) | — |
Secondary
| Measure | Time frame |
|---|---|
| Implementing a longitudinal register in order to examine the prognostic value of new biomarkers | — |
Countries
Germany
Contacts
Public ContactMustafa Yildirim
Universitätsklinikum Heidelberg/Innere III - Abteilung für Kardiologie, Angiologie und Pneumologie
Outcome results
None listed