The AIR-CPR Study: AI-Guided Chest Compressions

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age20+
SponsorFar Eastern Memorial Hospital

About this trial

The AIR-CPR project aims to improve survival rates for patients with Out-of-Hospital Cardiac Arrest (OHCA) by utilizing Artificial Intelligence (AI) to optimize chest compression locations. Current guidelines recommend a standardized compression point (the lower half of the sternum), yet recent research indicates that this position can compress the aortic valve in approximately 48.7% of patients, significantly reducing the chances of successful resuscitation.

This study will develop a deep learning model based on YOLO v8 to analyze real-time arterial pressure waveforms to identify proper aortic valve opening and closing. By identifying specific waveform features that humans cannot easily distinguish, the AI will guide rescuers to adjust the compression site-typically toward the left ventricle-to ensure optimal blood output. The project seeks to transform CPR from a standardized "one-size-fits-all" approach into a personalized, precision medicine intervention.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Adults aged 20 years or older.

Patients with out-of-hospital cardiac arrest (OHCA) undergoing 3.cardiopulmonary resuscitation (CPR) in the emergency department.

Disqualifiers

Pregnant patients.

Patients with obvious signs of death.

Patients with a signed "Do Not Resuscitate" (DNR) order.

Patients requiring extracorporeal cardio-pulmonary resuscitation (ECPR).

Trial population

The study population consists of adult patients experiencing non-traumatic out-of-hospital cardiac arrest who are transported to the Emergency Department of Far Eastern Memorial Hospital. This facility is the only medical center in New Taipei City and handles approximately 30% of the city's OHCA cases, ensuring a diverse and high-volume sample of patients receiving advanced life support.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • Device: AI-Enhanced Arterial Waveform Monitor (AIR-CPR App)

    Device

    A deep learning application based on the YOLO v8 architecture that analyzes real-time arterial pressure waveforms from a femoral A-line. It identifies whether the current chest compression location is causing aortic valve compression (as confirmed by TEE) and provides immediate feedback to the resuscitation team.

  • AI-Guided Chest Compression Repositioning

    Procedure/Surgery

    When the AI application indicates aortic valve compression, the rescuer adjusts the mechanical chest compression (LUCAS) position. Based on literature and AI feedback, the adjustment typically involves moving the compression point downward and toward the left parasternal line to avoid the aortic valve and optimize left ventricular output.

  • Transesophageal Echocardiography (TEE)

    Diagnostic test

    Used as the "Gold Standard" throughout the study. TEE is performed during CPR to record the actual opening and closing of the aortic valve and the deformation of cardiac chambers, providing the labels for AI training and the verification for clinical testing.

Treatment groups

255 Participants
are divided into 1 treatment group
Group A: OHCA Patients Receiving AI-Enhanced Resuscitation.3 interventions

Trial outcomes

Primary outcomes

1

AI Identification Accuracy of Aortic Valve Compression

The accuracy of the AI model in identifying whether the aortic valve is compressed or open during CPR, using Transesophageal Echocardiography (TEE) as the gold standard for verification.

Time frame
Collected during the clinical testing phase and feasibility assessment (Years 2 and 3).

Secondary outcomes

1

Successful Avoidance of Aortic Valve Compression

The percentage of cases where the resuscitation team successfully adjusted the chest compression location to stop aortic valve compression based on AI app feedback, confirmed by TEE.

Time frame
During the clinical feasibility assessment (Year 3).
2

Time Consumed for Compression Adjustment

The time interval between the first arterial waveform detection and the completion of the chest compression repositioning.

Time frame
During the clinical feasibility assessment (Year 3).
3

Rate of Return of Spontaneous Circulation (ROSC)

Incidence of ROSC and sustained ROSC (maintained for $\\ge 20$ minutes), as well as survival rates to hospital admission and discharge.

Time frame
From the start of the emergency department resuscitation until hospital discharge or death (up to approximately 30 days).
4

Favorable Neurologic Outcome at Discharge

Assessment of neurological status using the Cerebral Performance Category (CPC 1-2) or Modified Rankin Scale (mRS 0-2).

Time frame
At the time of hospital discharge (up to approximately 30 days).

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Far Eastern Memorial Hospital

Lead sponsor

National Health Research Institutes, Taiwan

Collaborator