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Clinical Trial Summary

This multi-center, prospective, cluster-randomized controlled trial will evaluate Mpirik automated notifications as an intervention to support identification and evaluation of patients possibly indicated for Aortic Valve Replacement (AVR). This study will evaluate the impact of Mpirik automated notifications on: (1) AVR utilization (including time to AVR); and (2) multidisciplinary heart team clinic evaluation (including time to evaluation) for patients with definitive or possible severe AS on echocardiogram. These endpoints will also be examined within and between assigned groups according to race, ethnicity, sex, and geography. The primary question that will be answered: Do automated alerts sent to clinical providers decrease under-treatment of severe aortic stenosis? The study will compare the rate of clinical follow-up and aortic valve surgery in a control group (no alerts sent) to a treatment group (alerts sent to an appropriate care provider).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06099665
Study type Interventional
Source Tempus AI
Contact Chris Rogers, BS
Phone (414) 220-4384
Email chris.rogers@tempus.com
Status Not yet recruiting
Phase N/A
Start date April 2024
Completion date December 2024

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