New registry tracks device safety in 1,000 blood clot patients
NCT ID NCT06600542
First seen Nov 01, 2025 · Last updated May 01, 2026 · Updated 29 times
Summary
This study is a global registry that will follow 1,000 adults who have already received treatment with an Inari Medical device for pulmonary embolism (blood clots in the lungs). The goal is to collect real-world data on device-related problems or serious side effects. No new treatments are being tested—just observation and data gathering.
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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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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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