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Pipeline Flex With SHield Technology Embolization - An International MulticEnter ObservationaL Post Market StuDy — SHIELD  

Intracranial Aneurysm Clinical Trial

Official title:
Pipeline Flex With SHield Technology Embolization - An International MulticEnter ObservationaL Post Market StuDy of Treated Intra Cranial Aneurysms (SHIELD)

Clinical Trial Summary

This is a prospective, single-arm, multi-center post-market observational study assessing the performance of the Pipeline™ Flex Embolization Device with Shield Technology™ in subjects undergoing treatment for intracranial aneurysms in a large real-world, post-market setting.

Clinical Trial Description

Eligible subjects will be treated with the Pipeline™ Flex Embolization Device with Shield Technology™. Subjects will undergo standard of care follow-up visits. Data generated per standard of care will be collected for 1 year beyond the index procedure. This clinical trial information was submitted voluntarily under the applicable law and, therefore, certain submission deadlines may not apply. (That is, clinical trial information for this applicable clinical trial was submitted under section 402 (j)(4)(A) of the Public Health Service Act and 42 CFR 11.60 and is not subject to the deadlines established by sections 402 (j)(2) and (3) of the Public Health Service Act or 42 CFR 11.24 and 11.44.) ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02719522
Study type Observational
Source Medtronic Neurovascular Clinical Affairs
Contact
Status Completed
Phase
Start date March 2016
Completion date August 22, 2019
View Details
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