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Kestra Medical Technologies to Present Late-Breaking ACE-PAS Trial Results at AHA 2025, Showcasing Next-Generation Wearable Defibrillator System

Key Takeaway: Kestra Medical Technologies will present results from the ACE-PAS Trial at the AHA 2025, showcasing their next-generation wearable cardioverter defibrillator system. This study, involving over 20,000 patients, evaluates the device's effectiveness in real-world settings. The late-breaking presentation highlights the significance of wearable defibrillator therapy in cardiac recovery.

Market Sentiment Analysis

POSITIVE FACTORS

  • Kestra's study selected for late-breaking presentation at AHA 2025.
  • ACE-PAS Trial is the largest prospective WCD study conducted to date.
  • The next-generation technology is gaining recognition in the cardiac recovery field.
  • The study aims to improve patient outcomes through innovative wearable technology.

Full Press Release Details

KIRKLAND, Wash., Nov. 04, 2025 (GLOBE NEWSWIRE) -- Kestra Medical Technologies, Ltd. (Nasdaq: KMTS), a wearable medical device and digital healthcare company, today announced its participation in the American Heart Association (AHA) Scientific Sessions 2025, to be held November 7–10 in New Orleans.
Kestra’s participation will include a late-breaking science presentation titledPrimary Results from the Post-Approval Study of a Next Generation Wearable Cardioverter Defibrillator System (ACE-PAS Trial), scheduled for Monday, November 10 at 8:44 a.m. CT in Session 211–213.
The ASSURE®WCD Clinical Evaluation Post-Approval Study (ACE-PAS) is a contemporary study designed to evaluate real-world experience with a next-generation wearable cardioverter defibrillator system. Enrolling more than 20,000 patients across the U.S., ACE-PAS represents the largest prospective WCD study conducted to date. Primary endpoints include overall shock conversion success and inappropriate shock rate, with additional measures evaluating first shock conversion success, median daily wear time, and false alarm rate. The study’s selection for AHA’s late-breaking science program underscores how wearable defibrillator therapy, and data-driven insights, are advancing the way clinicians approach cardiac recovery and risk protection.
“Being selected for a late-breaking presentation at AHA reflects both the clinical importance of the ACE-PAS study and the growing recognition of Kestra’s next-generation technology,” said Brian Webster, President and Chief Executive Officer of Kestra Medical Technologies. “As the cardiac recovery landscape evolves, we’re redefining how wearable monitoring and therapy integrates with connected care and digital health innovation—advancing patient protection and delivering deeper clinical insight.”
At booth #4617, attendees can explore the Kestra Cardiac Recovery System®, anchored by the ASSURE®Wearable Cardioverter Defibrillator, uniting proven patient protection with the clinical insights providers need to optimize guideline-directed medical therapy, implantable cardioverter defibrillator evaluation, and long-term recovery.
In addition to the late-breaking presentation, Kestra will host live demonstrations and discussions throughout the meeting, featuring an immersive in-booth experience that highlights the company’s leadership in advancing connected, data-driven solutions for cardiac recovery.
About KestraKestra Medical Technologies, Ltd. is a commercial-stage wearable medical device and digital healthcare company focused on transforming patient outcomes in cardiovascular disease using monitoring and therapeutic intervention technologies that are intuitive, intelligent, and connected. For more information, please visitwww.kestramedical.com.

Frequently Asked Questions

What is the ACE-PAS Trial?

The ACE-PAS Trial is a study evaluating a next-generation wearable cardioverter defibrillator system.

When will Kestra present at AHA 2025?

Kestra will present on November 10, 2025, at 8:44 a.m. CT.

How many patients are enrolled in the ACE-PAS Trial?

The trial has enrolled over 20,000 patients across the U.S.

What are the primary endpoints of the ACE-PAS Trial?

Primary endpoints include shock conversion success and inappropriate shock rate.

Last updated: Nov 4, 2025