New registry tracks device safety in blood clot patients
NCT ID NCT06600542
First seen Nov 01, 2025 · Last updated Jun 14, 2026 · Updated 37 times
Summary
This study is a registry that collects information from about 1,000 adults who have been treated for pulmonary embolism (a blood clot in the lungs) using Inari Medical devices. The goal is to monitor for any device-related or procedure-related side effects. Participants are not given any new treatment—they simply allow their medical data to be recorded after their standard procedure.
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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: •••••@•••••
Locations
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Azienda Ospedaliero Universitaria delle Marche
RECRUITINGAncona, Italy
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Great Western Hospital
RECRUITINGSwindon, United Kingdom
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Northwick Park Hospital
RECRUITINGLondon, United Kingdom
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Queen Elizabeth University Hospital
RECRUITINGGlasgow, United Kingdom
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Royal Free Hospital
RECRUITINGLondon, United Kingdom
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Royal London
RECRUITINGLondon, United Kingdom
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Royal Victoria Infirmary
RECRUITINGNewcastle, United Kingdom
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Santa Marta Hospital
RECRUITINGLisbon, Portugal
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Southmead Hospital Bristol
RECRUITINGBristol, United Kingdom
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UCLH University College London Hospital
RECRUITINGLondon, United Kingdom
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Conditions
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