US-based Acarix has initiated a real-world study that compares its AI-powered CADScor System’s clinical workflow efficiency with traditional stress tests to see which can identify patients with coronary artery disease (CAD) faster and improve the efficiency of emergency departments and clinics.
Acarix’s CADScor System has received de-novo clearance by the US Food and Drug Administration (FDA) and a European CE-mark.
The CADScor System is designed as a first-line diagnostic aid that uses acoustics and AI to analyse blood flow to rule out CAD. The system gives out results in under ten minutes and rules out CAD with at least 96% negative predictive value at the point of care.
The real-world data collection study is designed to assess potential cost-effectiveness, timesaving and a reduction in side effects by utilising the CADScor System to identify non-obstructive CAD in chest pain patients compared to traditional stress imaging tests.
The data for 200 patients with chest pain will be collected from the University of California, Davis, from both the emergency department and outpatient cardiology clinic. The enrolment is expected to start in Q2 this year.
Acarix expects the study data to be used to show the economic benefits of its CADScor System and raise awareness of the device.
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