Massive registry aims to make carotid stenting safer for stroke prevention
NCT ID NCT02240862
First seen Feb 20, 2026 · Last updated Jun 20, 2026 · Updated 20 times
Summary
This registry will follow 8,000 people with severe carotid artery disease who receive a stent to open the artery. The goal is to track how often strokes or deaths happen within 30 days after the procedure. The results will help select skilled doctors for a larger clinical trial testing stenting versus surgery.
Disclaimer
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This is a summary of
the original study
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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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University of Maryland - Administrative Center
RECRUITINGBaltimore, Maryland, 21201, United States
Contact
Contact Phone: •••-•••-•••• Email: •••••@•••••
What this could mean
Our plain-language read of the trial. This is informational only — not medical advice or a prediction.
Active substance
Carotid artery stent (a mesh tube placed in the neck artery to keep it open)
What this could lead to
If successful, this registry could help identify the best doctors and techniques for carotid stenting, potentially improving stroke prevention in future patients.
What could go wrong
This is an observational registry, not a treatment trial, so it won't directly test a new cure. Stenting carries risks like stroke or death within 30 days, and results may not apply to all patients.
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.