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Clinical Trial Summary

An observational post-market, open label, multicenter Observatory. The decision to use a WEB device to treat the patients has been made before and independently of the decision to include the patient in the French Observatory.


Clinical Trial Description

Subjects will be screened for Observatory eligibility after giving informed consent. The embolization procedure will be performed in the digital angiographic suite using standard angiographic techniques. Initial analysis of Observatory data will be performed at completion of 12 month follow-up for the first thirty-five (35) subjects. Subjects will be followed per Institution's standard of care. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01975233
Study type Observational
Source Microvention-Terumo, Inc.
Contact
Status Completed
Phase
Start date November 2012
Completion date December 2016

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