Sepsis
Conditions
Interventions
None listed
Sponsors
Chiba University Graduate School of Medicine
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Research subjects who are registered only in the databank must satisfy 1) and 3) below. For research subjects for whom specimens will be collected, all of the following 1), 2), and 4) must be met 1) Patients who have been diagnosed with sepsis according to the Sepsis-3 definition and admitted to the ICU 2) Patients who have given written consent to participate in the study (3) Research subjects who have not expressed their refusal to participate in this study after receiving an explanation of the study in a release of information document (opt-out document) 4) Adults who are at least 18 years of age, either as the person obtaining consent or as a surrogate.
Exclusion criteria
Exclusion criteria: 1) Research subjects who are not eligible for multidisciplinary treatment for sepsis 2) Research subjects who are judged by the investigator or others to be inappropriate for inclusion in the study 3) Subjects who have expressed their refusal to participate in this study through the information disclosure document.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 28-day survival, hospital survival, ICU survival, 90-day survival | — |
Secondary
| Measure | Time frame |
|---|---|
| Biomarkers and genetic polymorphisms that impact the severity of sepsis and its response to treatment | — |
Countries
Japan
Contacts
Public ContactOami Takehiko
Chiba University Graduate School of Medicine Department of Emergency and Critical Care Medicine
Outcome results
None listed