Heart failure device under the microscope: new registry tracks Real-World results
NCT ID NCT07098858
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study is a registry that will follow about 320 heart failure patients who receive the WiSE System, a device that helps the heart pump better. Researchers will watch for serious side effects within 30 days and check how well the device improves heart function and symptoms over time. The goal is to gather real-world data on safety and effectiveness.
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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.
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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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
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Study contacts
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
Locations
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Arrhythmia Research Group (St. Bernards Hospital)
RECRUITINGJonesboro, Arkansas, 72404, United States
Contact
Contact Email: •••••@•••••
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Naples Community Hospital
RECRUITINGNaples, Florida, 34102, United States
Contact
Contact Email: •••••@•••••
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Penn State Health
RECRUITINGHershey, Pennsylvania, 17033, United States
Contact
Contact
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University of Michigan
RECRUITINGAnn Arbor, Michigan, 48107, United States
Contact
Contact Email: •••••@•••••
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Weill Cornell Medicine
RECRUITINGNew York, New York, 10021, United States
Contact
Contact Email: •••••@•••••