burn, severe acute pancreatitis, sepsis
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: ->=20 years of age -Able and willing to provide informed consent -Patients with burn, severe acute pancreatitis or sepsis -Patients with KDIGO stage 1 screened -Patients who require continuous hemodiafiltration for more than 24 hours
Exclusion criteria
Exclusion criteria: -Pregnant women -Patients with chronic kidney disease or who received RRT before randomization -Patients with terminal cancer -Patients with body weight less than 30 kg -Patients considered ineligible for the study by the investigator
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| -Changes of scores (SOFA, SAPS2, APACHE2, DIC score, CAI) at 48 and 72 hours after enrollment | — |
Secondary
| Measure | Time frame |
|---|---|
| -Duration of mechanical ventilation in 28 days -Survival rate at 90 days -ICU stay days -Hospital stay days -Changes of plasma lactate and IL-6 level at 72 hours after continuous hemodiafiltration -Filter lifetime -Total fluid volume | — |
Countries
Japan
Contacts
Faculty of Medicine, Saga University Department of Emergency and Critical Care Medicine