An observational study in Exanguination, NCTH and Polytrauma, sponsored by Medical University of Graz. Recruiting at 1 site in Austria. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2025-04-17.
Sponsored by Medical University of Graz · Observational
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.
139 studies on the registry are indexed under Multiple Trauma; 32 are open to participants now.
This study's planned enrollment of 10 is below the median of 200 across 84 observational studies indexed under Multiple Trauma.
Browse Multiple Trauma studies →Medical University of Graz is the lead sponsor of 471 studies on the registry; 98 are open to participants now.
Counted across the registry records on this site, refreshed daily.
all patients meeting the eligibility criteria that are being transported to the rescucitation room of the Medical University of Graz
Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.
Exclusion Criteria:
effective 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
Plan to share: Undecided
No publications or documents are linked to this record.
Eligibility is decided by the study team. Share this record with your doctor or contact the team directly.
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