Resuscitative Endovascular Balloon Occlusion of the Aorta (REBOA) for the treatment of trauma patients in distress from torso hemorrhage; a prospective follow-up study in a Dutch level I trauma center
Recruiting
- Conditions
- Trauma patients who are treated using REBOA for presumed traumatic life-threatening hemorrhage or traumatic cardiac arrest.
- Registration Number
- NL-OMON25387
- Lead Sponsor
- Erasmus MC, University Medical Center Rotterdam, Trauma Research Unit Department of Surgery
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 30
Inclusion Criteria
1. Presented to Erasmus MC because of a physical trauma
2. Treatment attempted using REBOA (whether or not successful) for presumed traumatic life-threatening hemorrhage or traumatic cardiac arrest.
3. Provision of deferred informed consent (IC) by patient or proxy
Exclusion Criteria
No exclusion criteria apply.
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Whether REBOA was successful
- Secondary Outcome Measures
Name Time Method The time needed to obtain hemorrhage control with REBOA; Complications related to REBOA; General complications; Survival; REBOA procedure data; Patient demographics; Injury characteristics; Clinical parameters; Deployed resources and interventions; Hospital course.