Sepsis and septic shock
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Study types: randomized controlled trial (RCT). 2. Population: Patients no less than 18 years old and with sepsis based on any one of sepsis-1, sepsis-2, or sepsis-3 definitions. 3. Intervention: Intravenous esmolol or landiolol administration at any dose. 4. Control: Placebo or no intervention (without esmolol or landiolol administration).
Exclusion criteria
Exclusion criteria: studies not met inclusion criteria
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Short term mortality (in hospital mortality, 28 day mortality) | — |
Secondary
| Measure | Time frame |
|---|---|
| White blood cell count, troponin I, BNP, inflammatory marker and so forth Hemodynamic status(heart rate, blood pressure and so on) | — |
Countries
Japan,North America
Contacts
Fujita Health University School of Medicine Anesthesiology and critical care medicine