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Clinical Trial Summary

The investigators hypothesize that Arixtra patients will be less likely to experience wound infection than patients who have received low-molecular weight heparin, coumadin or aspirin with mechanical compression.


Clinical Trial Description

n/a


Study Design

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


Related Conditions & MeSH terms


NCT number NCT00909064
Study type Interventional
Source University of California, Davis
Contact Anto Fritz, M D
Phone 925 785 0826
Email atfritz@ucdavis.edu
Status Not yet recruiting
Phase Phase 4
Start date June 2009
Completion date December 2011

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