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Clinical Trial Summary

The objective of this study is to demonstrate equivalent hemostatic efficacy and safety between FS VH S/D and TISSEEL VH fibrin sealant in subjects undergoing cardiac surgery requiring cardiopulmonary bypass. If bleeding is still present after conventional surgical methods to achieve hemostasis have been applied FS VH S/D or Tisseel VH are applied. Achievement of hemostasis within 5 minutes is compared between the study groups.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT00161733
Study type Interventional
Source Baxter Healthcare Corporation
Contact
Status Completed
Phase Phase 3
Start date September 2002
Completion date November 2004

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