A41
Conditions
Interventions
Group 1: Patients who had been included in the SISPCT-trial are eligible for this study. A random sample is drawn from the original SISPCT study population for further analysis. From each of these pat
Sponsors
Universitätsklinikum Jena - Klinik für Anästhesiologie und Intensivmedizin
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Patients having participated in SISPCT-trial (independent of group assignment) IFNgamma-phenotyping available
Exclusion criteria
Exclusion criteria: Missing informed consent for biobanking
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Time-course of cGMP plasma-concentration in patients with sepsis | — |
Secondary
| Measure | Time frame |
|---|---|
| Time course of the components of the NO-sGC-cGMP-axis as well as the RAAS-system in plasma Time course of the proteom and markers of inflammation in plasma Correlation of the components of the NO-sGC-cGMP-axis as well as the RAAS-system and the proteom with vasopressor need, 28 day and 90 day mortality, IFNgamma-phenotype, and organ dysfunctions | — |
Countries
Germany
Contacts
Public ContactMichael Bauer
Universitätsklinikum Jena - Klinik für Anästhesiologie und Intensivmedizin
Outcome results
None listed