Heart failure device under the microscope: new registry launches

NCT ID NCT07098858

First seen Nov 21, 2025 · Last updated May 16, 2026 · Updated 18 times

Summary

This study is a registry that will follow about 320 people with heart failure who receive the WiSE System, a device that helps the heart pump better. The goal is to see how safe and effective the device is in real-world use by tracking side effects and heart function improvements. Participants must be eligible for the device and agree to follow-up visits.

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This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.

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Contacts and locations

Study contacts

  • Contact

    Phone: •••-•••-•••• Email: •••••@•••••

Locations

  • Arrhythmia Research Group (St. Bernards Hospital)

    RECRUITING

    Jonesboro, Arkansas, 72404, United States

    Contact

    Contact Email: •••••@•••••

  • Naples Community Hospital

    RECRUITING

    Naples, Florida, 34102, United States

    Contact

    Contact Email: •••••@•••••

  • Penn State Health

    RECRUITING

    Hershey, Pennsylvania, 17033, United States

    Contact

    Contact

  • University of Michigan

    RECRUITING

    Ann Arbor, Michigan, 48107, United States

    Contact

    Contact Email: •••••@•••••

  • Weill Cornell Medicine

    RECRUITING

    New York, New York, 10021, United States

    Contact

    Contact Email: •••••@•••••

Conditions

Explore the condition pages connected to this study.