Brain aneurysm device registry aims to improve patient outcomes
NCT ID NCT06215105
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 2 times
Summary
This study is a registry that will collect real-world data from 750 people with brain aneurysms treated with MicroVention devices. The goal is to see how well these devices work and how safe they are in everyday medical practice. Participants will be followed for at least one year to check aneurysm closure and any complications.
What this could mean
Our plain-language read of the trial. This is informational only — not medical advice or a prediction.
- Active substance
- Intracranial aneurysm treatment devices (MicroVention)
- What this could lead to
- If successful, this registry could provide real-world evidence on how well these devices work and their safety, helping doctors make better treatment decisions for brain aneurysms.
- What could go wrong
- This is an observational registry, not a controlled trial, so results may be influenced by patient selection and other factors. It does not test a new treatment, only collects data on existing devices.
This is an AI summary of the original study and may miss details. Read our disclaimer.
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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
Locations
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Abbott Northwestern Hospital
Minneapolis, Minnesota, 55407, United States
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Albany Medical Center
Albany, New York, 12208, United States
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Memorial Healthcare System
Hollywood, Florida, 33021, United States
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Orlando Health
Orlando, Florida, 32806, United States
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University of Iowa
Iowa City, Iowa, 52242, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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