Sepsis
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: We included trials with the following characteristics: 1. Study type: RCT. 2. Patient population: Patients aged above or equal to 18 years with sepsis based on any one of Sepsis-1, Sepsis-2, or Sepsis-3 definitions. 3. Intervention: Intravenous high-dose vitamin C (greater than or equal to 1.5g every 6 hours or 25mg/kg every 6 hours) 4. Control: Placebo or no intervention.
Exclusion criteria
Exclusion criteria: We excluded articles that included patients <18 years, published in non-English and are conference proceedings.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Short term mortality including 28-day mortality, 30-day mortality, or in-hospital mortality | — |
Secondary
| Measure | Time frame |
|---|---|
| ICU length of stay Hospital length of stay Duration of vasopressors Delta SOFA at 72-96 hours Ventilator-free days Adverse events Sub-group analysis based on mean/median control SOFA score. Sub-group analysis based on HAT therapy vs. non-HAT therapy. | — |
Countries
Japan,North America
Contacts
Cleveland Clinic Critical Care Medicine