Abdominal Aortic Tourniquet Application for Non-Traumatic Out-of-Hospital Cardiac Arrest

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorKlinikum Klagenfurt am Wörthersee

About this trial

The aim of the study is to investigate whether occluding the abdominal aorta with an external device could be a potential therapeutic option in cases of non-traumatic cardiac arrest occurring outside of a hospital.

In cardiac arrest, the heart suddenly stops beating, causing the circulation of blood to collapse. In this situation, vital organs-especially the brain and the heart itself-are no longer adequately supplied with oxygen. Without immediate treatment, severe damage or death occurs within minutes.

The study therefore examines a specific intervention: the temporary occlusion of the abdominal aorta, which carries blood to the lower regions of the body. If this artery is blocked for a short period, the available blood can be redirected more effectively to the upper parts of the body. In theory, this could improve the oxygen supply to these organs and increase the likelihood that the heart will resume beating or that neurological damage can be reduced.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Cardiac arrest with indication for initiation of resuscitation

Age ≥ 18 years

Disqualifiers

Pregnancy (suspected or confirmed)

Age < 18 years

Abdominal circumference does not allow application of the AAJT

Traumatic etiology

Trial design

Design model

Single group

Treatments tested in this trial

  • Abdominal Aortic Junction Tourniquet in non-traumatic out-of-hospital cardiac arrest

    Device

    If a patient is found in cardiac arrest, eligibility is assessed. If the patient is deemed eligible, the following steps are performed: 1. Initiation of standard Advanced Cardiac Life Support (ACLS) 2. Endotracheal intubation and controlled mandatory ventilation according to ERC 2025 guidelines 3. Initiation of mechanical CPR 4. Arterial cannulation of an artery in the left upper extremity; access via the right upper extremity may be attempted after two unsuccessful attempts 5. Exclusion of reversible causes based on clinical history, physical examination, and/or ultrasound 6. Inflation of the AAJT 7. Device removal and termination of resuscitation (TOR) if ERC criteria are met 8. If return of spontaneous circulation (ROSC) is achieved, the AAJT remains in place until normotension is established, either spontaneously or with vasopressor support

Treatment groups

5 Participants
are divided into 1 treatment group
Group A: Abdominal aortic occlusion by AAJT ApplicationExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Time from initiation of AAJT application to complete inflation

Time frame
1 hour

Secondary outcomes

1

Time from dispatch to application

Time frame
1 hour
2

time from arrival on scene to application

Time frame
1 hour
3

time from initiation of resuscitation to application

Time frame
1 hour
4

change in end-tidal CO₂ (etCO₂) measured in mmHg

Time frame
1 hour

Other outcomes

1

In patients admitted to the hospital with ROSC who underwent CT of the thorax and abdomen: percentage of patients with intrathoracic injuries; percentage of patients with intra-abdominal injuries

Analysis of the CT-report with regards to findings of device related intrathoracic or intraabdominal injuries

Time frame
30 days
2

In patients without ROSC in whom an autopsy was performed: percentage of patients with intrathoracic injuries; percentage of patients with intra-abdominal injuries

Analysis of the autopsy-report with regards to findings of device related intrathoracic or intraabdominal injuries

Time frame
30 days

Sponsors and contacts

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This trial is not recruiting at the moment. You can still explore other options: