Evaluation of Efficacy and Safety of Resuscitative Endovascular Balloon Occlusion of the Aorta with standardized protocol; A prospective observational study
Not Applicable
- Conditions
- Refractory hemorrhagic shock
- Registration Number
- JPRN-UMIN000029760
- Lead Sponsor
- Chiba University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 150
Inclusion Criteria
Not provided
Exclusion Criteria
Age <15 years old The patients undergoing resuscitative thoraacotomy, elective cases, REBOA catheter placement without inflation
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 24 hour and 30 day mortality Transfusion within first 24 hours
- Secondary Outcome Measures
Name Time Method