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Abdominal Aortic Junction Tourniquet (AAJT-S) for Non-compressible Torso Haemorrhage

M

Medical University of Graz

Status

Enrolling

Conditions

NCTH
Exanguination
Polytrauma

Study type

Observational

Funder types

Other

Identifiers

NCT06622317
1063/2024

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

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.

Enrollment

10 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 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)
  • is thought to benefit from trauma resuscitation with AAJT-S or REBOA zone III

Exclusion criteria

  • suspected additional bleeding source proximal to the umbilicus, or
  • known or suspected pregnancy at presentation, or
  • known abdominal aortic aneurysm

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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