New artery-closing device tested for ECMO patients
NCT ID NCT07019662
First seen Nov 01, 2025 · Last updated Jun 13, 2026 · Updated 29 times
Summary
This study compares a suture-based device to standard methods (manual compression or surgery) for closing the artery after removing ECMO tubes in patients with severe heart and lung failure. About 102 adults will be randomly assigned to either the device or standard care. The goal is to see if the device is as safe and effective at preventing complications like bleeding or vessel injury.
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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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Contacts and locations
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Study contacts
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
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Contact
Locations
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Universitäres Herz- und Gefäßzentrum Frankfurt ZIM - Med. Clinic 3 - Cardiology and Angiology
RECRUITINGFrankfurt, Germany
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Universitätsmedizin der Johannes Gutenberg-Universität Mainz - Zentrum für Kardiologie
RECRUITINGMainz, Germany
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.