Acute respiratory distress syndrome
Conditions
Interventions
control group:placebo
Sponsors
Affiliated Hospital of Jiangsu University
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. All adult patients (aged >= 18 years); 2. With a diagnosis of ARDS; 3. Patients voluntarily participate in the experiment.
Exclusion criteria
Exclusion criteria: 1. Pregnant or lactating women; 2. Expected to die within 48 hours; 3. Had a history of immune disease or long-term admission of immunosuppressive drug; 4. Patients with cardiogenic pulmonary edema.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| IL-6;TNF-a;IL-1ß;sIgA; | — |
Secondary
| Measure | Time frame |
|---|---|
| Oxygenation index;Mechanical ventilation time; | — |
Countries
China
Contacts
Public ContactYin Jiangtao
Affiliated Hospital of Jiangsu University
Outcome results
None listed