Sepsis
Conditions
Interventions
experimental group:use of medicine
Placebo group:use of placebo
Sponsors
State Key Laboratory of Trauma, Burns, and Combined Injury, Department 1, Research Institute of Surgery, Daping Hospital, The Third Military Medical University
Eligibility
Sex/Gender
All
Age
18 Years to 76 Years
Inclusion criteria
Inclusion criteria: Sepsis group: 1. Aged 18-76 years male and female; 2. Patients in ICU (diagnosed with sepsis or suspected sepsis or severe infection with organ damage patients); 3. Signing of the letter of informed consent. Non-sepsis group: including healthy people, patients with infections or trauma.
Exclusion criteria
Exclusion criteria: 1. patients with blood system diseases, abnormal lipid metabolism, and infectious diseases 2. pregnant and lactating women; 3. patients with mental disorders; 4. refuse to sign informed consent and refuse to provide information.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Incidence of sepsis;Mortality of sepsis; | — |
Secondary
| Measure | Time frame |
|---|---|
| health related quality of life score;Critical Illness score;hemodynamic parameters;Biochemical target; | — |
Countries
China
Contacts
Public ContactHuaping Liang
Research Institute of Surgery, Daping Hospital, Army Military Medical University
Outcome results
None listed