I63 I64
Conditions
Interventions
Group 1: Prospective observational study. Laboratory samples taken during routine clinical practice that are no longer needed for routine clinical purposes are stored at two points in time (V1 and V2)
Sponsors
Medizinische Hochschule Hannover
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: -written informed consent -imaging confirmed ischemic stroke, but not older than 14 days at admission -available reserve blood sample
Exclusion criteria
Exclusion criteria: not available
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Primary endpoint: Embolic stroke of undetermined source (ESUS) vs. all other stroke etiologies according to TOAST, determined at the time of discharge. The endpoint is assessed by evaluating the data to be collected in the study protocol. The endpoint was assessed in 10% of patients by two independent stroke experts using randomization. | — |
Secondary
| Measure | Time frame |
|---|---|
| Differences in genetic stroke risk variants, clinical parameters, and circulating biomarkers between stroke etiologies | — |
Countries
Germany
Contacts
Public ContactJohanna Ernst
Medizinische Hochschule Hannover
Outcome results
None listed