End-stage liver disease
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1.Patients scheduled for liver transplantation in this hospital. 2.ASA classification Grade I - IV; 3.Aged 18-65 years, regardless of gender; 4.Able to communicate effectively and willing to participate in this study;
Exclusion criteria
Exclusion criteria: 1.Untreated stage 2 and stage 3 hypertension; 2.Known allergies to eggs, soy products, propofol, or ciprofol; 3.Other reasons that make the investigator believe the patient is not suitable for inclusion in the clinical trial;
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The dosage of norepinephrine used during the anesthesia induction period.; | — |
Secondary
| Measure | Time frame |
|---|---|
| The average degree of fluctuation of systemic vascular resistance index during the anesthesia induction period.;The fluctuation of mean arterial pressure during the anesthesia induction period.;The maximum decrease in mean arterial pressure.;The average degree of fluctuation of the cardiac index during the anesthesia induction period.;Blood lactic acid levels during the anesthesia induction period; | — |
Countries
China
Contacts
The First Affiliated Hospital,Sun Yat-sen University