COVID-19
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. able to provide informed consent 2. Individuals who have been infected and had a mild COVID-19 disease (reconvalescents). These individuals had typical symptoms for at least 5 days but have never been treated in the hospital. These individuals are fully receovered at study inclusion. 3. Individuals who have been infected and had a severe COVID-19 disease (reconvalescents). These individuals were hospitalized for COVID-19 disease. These individuals are fully receovered at study inclusion. 4. Healthy volunteers never infected with SARS-CoV-2 (control group).
Exclusion criteria
Exclusion criteria: 1. Intake (regular or acute within 7 days of blood sample) of drugs interfering with platelet function (e.g. acetyl salicylic acid, ibuprofen, antidepressants of SSRI and SSNRI class). 2. platelet dysfunction or thrombocytopenia 3. pregancy and lactation period
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Difference in platelet activation measured by light transmission aggregation | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Formation of thrombin by Calibrated Automated Thrombogram 2. Determination of specific markers of platelet activation (e.g. CD62, PAC1) 3. Determination of platelet surface markers Bestimmung von (e.g. CD62, CD63, GPVI, HLA) 4. Influence of MRP4 inhibition with Ceefourin-1 on pletelet function 5. MRP4 expression and factors of S1P metabolism in pletelets 6. S1P concentrationen and thromboxan B2 concentration in plasma 7. pletelet count 8. SARS-CoV-2 antibodies in serum | — |
Countries
Germany
Contacts
Institut für Pharmakologie, Universitätsmedizin Greifswald