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Abdominal Aortic Junction Tourniquet (AAJT-S) for Non-compressible Torso Haemorrhage in the Prehospital and Emergency Room Setting

M

Medical University of Graz

Status

Not yet enrolling

Conditions

NCTH
Exanguination
Polytrauma

Study type

Observational

Funder types

Other

Identifiers

NCT07274150
1331/2025

Details and patient eligibility

About

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.

Full description

Much like REBOA, AAJT-S can potentially stop blood flow distal to the device and therefore improve proximal aortic perfusion, minimize haemorrhage and stabilize patients until definite surgical repair/bleeding control is feasible. In contrast to REBOA, there is no need of femoral access and therefore, appropriate training is easily achieved.

This study seeks to gather further information on the benefits and potential harms of this intervention on a multicentre level.

Enrollment

50 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Written consent of the participant after being informed
  2. Aged, or believed to be aged, 18 years or above
  3. Confirmed or suspected life-threatening lower body trauma (i.e. signs of inadequate perfusion of tissues, tachycardia, hypotension, suspected blood loss)
  4. Thought to benefit from trauma resuscitation with AAJT-S or REBOA zone III
  5. Traumatic cardiac arrest

Exclusion criteria

-

Trial contacts and locations

1

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Central trial contact

Gabriel Honnef, MD, PhD

Data sourced from clinicaltrials.gov

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