sepsis Liver failure (liver transplant patients)
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: • Inclusion criteria:;o Age 18 years or older.;o Informed consent of the test person or from her/his lawful representative.;o Patients admitted for liver transplant, hemi-hepatectomy for primary or secondary liver malignancy, or sepsis. ;The control group will be recruited from patients admitted for subarachnoid bleeding without liver disease.
Exclusion criteria
Exclusion criteria: • Exclusion criteria:;o No informed consent.;o Allergy for the administered substances, including inborn errors of the *fructose-pathway*.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Primary study objectives; The main study objective is the clinical use of D-sorbitol plasma clearance as a measure of functional liver blood flow. | — |
Secondary
| Measure | Time frame |
|---|---|
| Not applicable. | — |
Countries
Netherlands