A41 K72
Conditions
Interventions
Group 1: Estimation of the liver function in septic patients with LiMAx-Test
Sponsors
Charitè - Universitätsmedizin Berlin - Campus Virchow
Klinik für Allgemein-, Viszeral- und Transplantationschirurgie
Eligibility
Sex/Gender
All
Age
18 Years to 80 Years
Inclusion criteria
Inclusion criteria: Bacterial Sepsis Inform consent present
Exclusion criteria
Exclusion criteria: Allergy against ICG or Methacetin Chemotherapy in the last 8 weeks Immunosuppression (Equivalent of Cortison >5mg) Advanced liver dysfunction prior to actual disease Any organ transplantation HIV Pregnancy, breast feeding Absent inform consent Factors, limitating the ability of patients to cooperate during study (e. g. reduced mental function, drug abuse)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Correlation between result of the Maximal Liver Function Capacity Test (LiMAx-Test) the mortality rate | — |
Secondary
| Measure | Time frame |
|---|---|
| Comparison of the result of the Maximal Liver Function Capacity Test (LiMAx-Test) with the Indocyaningreen plasmadilution rate and other parameter for assessment of the liver function (transaminases, bilirubine, coagulation-tests, zxtokines) Length of stay in intensive care unit Lenght of stay in hospital | — |
Countries
Germany
Contacts
Public ContactMagnus Kaffarnik
Charite - Universitätsmedizin Berlin, Campus Virchow Klinik für Allgemein, Viszeral- und Transplantationschirurgie
Outcome results
None listed