stroke
Conditions
Interventions
None listed
Sponsors
Erasmus MC, Universitair Medisch Centrum Rotterdam
Eligibility
Age
18 Years to 64 Years
Inclusion criteria
Inclusion criteria: - Subjects should sign up voluntarily - Subjects should be healthy - Subjects should be between 18 and 70 years old - Subjects should give written informed consent
Exclusion criteria
Exclusion criteria: - Subjects with diseases known to affect coagulation (e.g. cancer, diabetes, cardiovascular disease) - Subjects using medication interfering with coagulation
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Blood from healthy volunteers will be used as a source for red blood cells, platelets, immune cells, fibrinogen, plasma. Using these components, we will optimize to generate clot analogues of various composition for mechanical testing and imaging. The main study endpoints will be to establish and quantify the relationship between clot composition -for both homogeneous and heterogeneous clost- and the -global and local- mechanical properties and imaging features. | — |
Secondary
| Measure | Time frame |
|---|---|
| Not applicable. | — |
Countries
Netherlands
Outcome results
None listed