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Clinical Trial Summary

Subjects with anterior acute STEMI who receive an IABC before primary PCI will have decreased MI size.


Clinical Trial Description

Post clearance device study in which subjects with acute MI will be randomized 1:1 to either receive IAB or to receive standard of care without IAB before mechanical reperfusion. Subjects will be followed throughout their hospital stay and at 30 days. ;


Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00833612
Study type Interventional
Source Datascope Corp.
Contact
Status Completed
Phase Phase 4
Start date December 2008
Completion date March 2011

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