I25.9
Conditions
Interventions
Group 1: Blood Samples from Patients on Clopidogrel Therapy will be used for in-vitro addition of platelet concentrate equivalents.
Group 2: Blood Samples from Patients on Prasugrel Therapy will be u
Sponsors
Medizinische Universität Wien
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Patients on Clopidogrel, Prasugrel or Ticagrelor + Aspirin Therapy
Exclusion criteria
Exclusion criteria: inadequate ADP Receptor inhibition while on Clopidogrel/Prasugrel/Ticagrelor Therapy
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| AUC (ADP) in Multiple Electrode Aggregometry prior to and after the Transfusion of 2 or 4 Platelet Concentrate Equivalents | — |
Secondary
| Measure | Time frame |
|---|---|
| AUC (TRAP & ASPI) in Multiple Electrode Aggregometry prior to and after the Transfusion of 2 or 4 Platelet Concentrate Equivalents | — |
Countries
Austria
Contacts
Public ContactDieter Adelmann
Medizinische Universität Wien
Outcome results
None listed