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Clinical Trial Summary

The objective of this post-market registry is to assess technical efficacy and safety associated with the use of the BOSS Balloon Guide Catheter during neuro-vascular procedures while providing temporary arrest of blood flow.


Clinical Trial Description

This is a prospective, multi-center, non-randomized observational registry evaluating use of BOSS balloon guide catheters in patients diagnosed with an acute ischemic stroke due to large intracranial vessel occlusion. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04416659
Study type Observational [Patient Registry]
Source Medtronic Neurovascular Clinical Affairs
Contact
Status Completed
Phase
Start date January 12, 2021
Completion date October 27, 2021

See also
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