Brain aneurysm device study halted early
NCT ID NCT04391803
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looked at a device called the Pipeline Flex Embolization Device with Shield Technology to treat ruptured brain aneurysms that are hard to fix with surgery or coils. The goal was to see if it could safely block the aneurysm and prevent rebleeding. The study was stopped early, and only 25 people were enrolled.
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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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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
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Locations
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Geisinger Medical Center
Danville, Pennsylvania, 17822, United States
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Rush University Medical Center
Chicago, Illinois, 60612, United States
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Semmes Murphey Clinic
Memphis, Tennessee, 38120, United States
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Stony Brook University Hospital
Stony Brook, New York, 11794, United States
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University of Kentucky Albert B Chandler Hospital
Lexington, Kentucky, 40506, United States
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Wellstar Kennestone Hospital
Marietta, Georgia, 30060, United States
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Yale New Haven Hospital
New Haven, Connecticut, 06510, United States