Pipeline Embolization Device (PED)
Device1 or more PEDs placed in the parent artery of the affected aneurysm via endovascular approach.
Other names: Pipeline Embolization Device, PED
NCT Number: NCT00777907
To compare the safety and effectiveness of Pipeline Embolization Device to coil embolization for the treatment of coilable wide-necked intracranial aneurysms
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Notify Me21 year–75 year
All sexes
Interventional
Phase 3
Barrow Neurological Institute, Phoenix, Arizona, United States
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
1 or more PEDs placed in the parent artery of the affected aneurysm via endovascular approach.
Other names: Pipeline Embolization Device, PED
Placement of bare platinum coils into the target aneurysm with balloon remodeling allowed.
Time frame: 180 days
Time frame: 1, 3 and 5 years
Time frame: 180 days
Time frame: 180 days, 1, 3 and 5 years
Time frame: 180 days, 1, 3 and 5 years
Time frame: 180 days
Chestnut Medical Technologies
Industry
Acronym: COCOA
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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