This study seeks to evaluate the feasibility of a Abdominal Aortic Balloon Occlusion of the Aorta (AAJT-S) in exanguinating trauma patients with non-compressible truncal haemorrhage in the emergency room and the pre-hospital setting.
The study is designed as a prospective observational study to accomapany the impementation of this device in clinical routine. However, the device has already been used in the emergency room and AAJT-S application is no study specific intervention.
Study Type
OBSERVATIONAL
Enrollment
10
Medical University of Graz
Graz, Styria, Austria
RECRUITINGeffective placement of the device
cessation of bloodflow distal to the device
Time frame: 1 hour
30-day mortality
in-hospital
Time frame: 30 days
Complications
Occurrence of complications of device application
Time frame: 90 days
Heart rate
Improvement (reduction) in beats/minute
Time frame: 1 hour
Base excess
Improvement (reduction) in mmol/l
Time frame: 1hour
Blood pressure (systolic and diastolic)
Improvement in mmHg
Time frame: 1 hour
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