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.
Written consent of the participant after being informed
Aged, or believed to be aged, 18 years or above
Confirmed or suspected life-threatening lower body trauma (i.e. signs of inadequate perfusion of tissues, tachycardia, hypotension, suspected blood loss)
Thought to benefit from trauma resuscitation with AAJT-S or REBOA zone III
None
1. Suspected additional bleeding source proximal to the umbilicus 2. Known or suspected pregnancy at presentation 3. Known abdominal aortic aneurysm
Cohort
Prospective
Not listed
effective placement of the device
cessation of bloodflow distal to the device
Outcome Measure
30-day in hospital mortality
Complications
Occurrence of complications of device application
hemodynamic improvement after application
lower hart rate / higher blood pressure (improvement in bpm/mmHg)
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This trial is not recruiting at the moment. You can still explore other options:
