CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 108 enrolled
Drug / intervention
Pipeline Embolization Device (PED)device
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00777088
NCT00777088N/ACompleted
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Pipeline for Uncoilable or Failed Aneurysms

Medtronic Neurovascular Clinical Affairs·interventional·Posted Oct 22, 2008·Updated Nov 20, 2018

In Brief

A clinical study evaluating Pipeline Embolization Device (PED) for Intracranial Aneurysm. Completed, enrolled 108 participants across 10 sites in 3 countries.

Detailed Summary

To determine the safety and effectiveness of Pipeline Embolization Device for the treatment of uncoilable or failed wide-necked intracranial aneurysms (IA).

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsIntracranial Aneurysm
CountriesHungary, Turkey (Türkiye), United States
Collaborators--

Timeline

N/ACompletedFinished
200920102011201220132014201520162017201820192020202120222023202420252026
First PostedOct 22, 2008
Enrollment StartOct 1, 2008
Primary CompletionSep 22, 2014
TodayJul 2, 2026
Enrollment to primary: 6.0 yearsPosted 17.7 years ago

Interventions

Pipeline Embolization Device (PED)device

1 or more PEDs placed in the parent artery of the affected aneurysm via endovascular approach