CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 197 enrolled
Drug / intervention
Pipeline™ Embolization Device/ Pipeline™Flex Embolization Devicedevice
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/NCT02186561
NCT02186561N/ACompleted
CompareCT.gov

Prospective Study on Embolization of Intracranial Aneurysms With the Pipeline™ Device (PREMIER)

Medtronic Neurovascular Clinical Affairs·interventional·Posted Jul 10, 2014·Updated Dec 27, 2019

In Brief

A clinical study evaluating Pipeline™ Embolization Device/ Pipeline™Flex Embolization Device for Intracranial Aneurysm. Completed, enrolled 197 participants across 23 sites in 2 countries.

Detailed Summary

The purpose of this study is to assess the safety and effectiveness of the Pipeline™ device in the treatment of unruptured, wide-neck intracranial aneurysms.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsIntracranial Aneurysm
CountriesCanada, United States
Collaborators--

Timeline

N/ACompletedFinished
201520162017201820192020202120222023202420252026
First PostedJul 10, 2014
Enrollment StartJul 24, 2014
Primary CompletionNov 18, 2016
Study CompletionDec 13, 2018
TodayJul 2, 2026
Enrollment to primary: 2.3 yearsPosted 12.0 years ago

Interventions

Pipeline™ Embolization Device/ Pipeline™Flex Embolization Devicedevice