A multicenter, prospective observational study for the epidemiology of severe trauma
Not Applicable
- Conditions
- Trauma
- Registration Number
- JPRN-UMIN000019588
- Lead Sponsor
- Japanese Association for Acute Medicine
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 500
Inclusion Criteria
Not provided
Exclusion Criteria
Out of hospital cardiac arrest
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 28-day mortality
- Secondary Outcome Measures
Name Time Method ICU free days Ventilator free days 24-hour amount of blood transfusion Subsequent Acute Respiratory Distress Syndrome (ARDS)