A40 A41 R65
Conditions
Interventions
Group 1: Sampling: 6 blood probes from 3 successive days starting with date of suspected sepsis.
Measures: RT-DC, CRP, PCT, IL-6
Sponsors
Institute of Bioinformatics, University Medicine Greifswald
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Intensive care patient with suspected sepsis
Exclusion criteria
Exclusion criteria: none
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Analysis of the RT-DC parameters / cell deformation, especially of the leukocytes in the clinical course (analysis of the kinetics), which are characterized by changes in cell size, deformation and brightness, in relation to the actual sepsis onset. | — |
Secondary
| Measure | Time frame |
|---|---|
| RT-DC measurements at different times to analyze the same blood sample 1h, 2h, 4h, 8h after blood sampling to clarify the questions: How quickly does the fresh blood have to be analyzed? How stable are the measurements? Comparison of the RT-DC parameters with proven infection parameters CRP, PCT, IL-6 (correlation analysis, analysis of the significance of the new parameters) | — |
Countries
Germany
Contacts
Public ContactMatthias Gründling
Qualitätsmanagementprojekt Sepsisdialog, Universitätsmedizin Greifswald, Klinik und Poliklinik für Anästhesiologie und Intensivmedizin
Outcome results
None listed