Septic Shock
Conditions
Interventions
Group 1: Randomization: early elimination of cytokines via Cytosorb
Group 2: Randomization: no Cytosorb
Group 3: Observational group, no randomization: patients with septic shock but without possibili
Sponsors
Universitätsklinikum Würzburg
Eligibility
Sex/Gender
All
Age
18 Years to 85 Years
Inclusion criteria
Inclusion criteria: Septic shock with hyperinflammation, Age > 18y, written consent
Exclusion criteria
Exclusion criteria: Age > 85y, acute coronary syndrome, severe drug-induced immunosuppression, fatal co-morbidity
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Reduction of cumulative vasopressor-dose after 72h | — |
Secondary
| Measure | Time frame |
|---|---|
| Moleculare analyses of humoral and celullar immune responses, organ dysfunction, length of mechanical ventilation, length of ICU stay | — |
Countries
Germany
Contacts
Public ContactChristopher Lotz
Universitätsklinikum Würzburg
Outcome results
None listed