Acute respiratory distress syndrome (ARDS)
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Adult patients aged >=18 years and <85 years, with no restrictions on race, nationality and gender; 2. The research complies with the Declaration of Helsinki and China's clinical trial research regulations, and the patients or their family members are informed and agree to participate in the trial; 3. Patients who met ARDS criteria when admitted to the ICU or during their stay in the ICU.
Exclusion criteria
Exclusion criteria: 1. Deformity of the thoracic cavity; 2. There are any contraindications to the use of EIT (such as automatic implantable cardioverter defibrillators and implantable pumps); 3. Hypernatremia (serum sodium exceeds 145mmol/L); 4. Pregnancy or lactation; 5. Patients who have been included in this study, or patients who are participating in other studies during the same period; 6. Patients or their family members refused this study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Proportion of areas with uniform ventilation and perfusion in EIT images; | — |
Secondary
| Measure | Time frame |
|---|---|
| 28-day mortality;Ventilator-free time; | — |
Countries
China
Contacts
Sichuan Provincial People's Hospital