Acute Coronary Syndrome Clinical Trial
Official title:
Generic and Branded Enoxaparin Bioequivalence: a Randomized Study in Acute Coronary Syndrome Patients With an In-vitro Thrombin Generation Testing Comparison
Because of their anti-Xa and ease of administration activity, the Low molecular weight
heparin represent an attractive alternative to the unfractionated heparin. Several clinical
trials have demonstrated that Low molecular weight heparin was more effective than
Unfractionated heparin without increasing bleeding complications. Enoxaparin has been the
most studied. Its use is recommended.
Demonstrate that Enoxa® is comparable to that of Lovenox® in the anti-Xa activity action.
Single-center randomized controlled trial, single-blind, including patient with an acute
coronary syndrome confirmed, to measure the anti-Xa activity between H0 and H4.the study was
done on two groups ; ENOXA® group : In this case the patient is given an injection of
enoxaparin ( ENOXA® ; UNIMED Laboratories) intravenously. Curative dose (100 IU/10 kg).
Control group ( LOVENOX ® ):
In this case the patient receives LOVENOX intravenous injection curative dose of 100 kg IU/10
.
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