New heart pump aims to make risky artery procedures safer

NCT ID NCT04477603

First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study tests a temporary heart pump called Impella ECP in 100 adults undergoing high-risk angioplasty. The pump helps maintain blood flow during the procedure. Researchers are checking if the device is safe and works as intended, with follow-up for 30 days after the procedure.

What this could mean

Our plain-language read of the trial. This is informational only — not medical advice or a prediction.

Active substance

Impella ECP (a temporary heart pump device)

What this could lead to

If successful, this device could provide safer hemodynamic support during high-risk angioplasty, potentially reducing complications.

What could go wrong

This is an early feasibility study with only 100 participants, so results may not apply broadly. The device carries risks like bleeding or vessel damage.

Disclaimer Read more

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.

coronary artery disorder

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Henry Ford Health St. John Hospital

    Detroit, Michigan, 48236, United States

  • Henry Ford Hospital

    Detroit, Michigan, 48202, United States

  • The Christ Hospital

    Cincinnati, Ohio, 45219, United States

  • The Valley Hospital

    Paramus, New Jersey, 07652, United States

  • Tufts Medical Center

    Boston, Massachusetts, 02111, United States