767
Participants
Start Date
October 11, 2020
Primary Completion Date
June 8, 2021
Study Completion Date
June 8, 2021
Soluble Urokinase Plasminogen Activator Receptor
Participants will undergo sampling of peripheral venous blood, immediately after admission. Blood samples drawn from all patients and EDTA plasma will be stored at -80° C until later measurement. Plasma suPAR levels will be determined using the suPARnostic® ELISA assay (ViroGates, Denmark), which is based on a simplified double monoclonal antibody sandwich ELISA assay whereby samples and peroxidase-conjugated anti-suPAR are first mixed together and then incubated in anti-suPAR pre-coated micro wells. The recombinant suPAR standards of the kit are calibrated against healthy human blood donor samples. suPAR concentrations are determined as ng/mL plasma.
University Hospital of Larisa, Department of Anesthesiology, Larissa
University of Thessaly
OTHER