drugset / Trial / NCT00077792

Enoxaparin and Thrombolysis Reperfusion for Acute Myocardial Infarction Treatment Thrombolysis in Myocardial Infarction - Study 25 (ExTRACT-TIMI25)

NCT00077792 ↗

Phase 3 Completed 20506 enrolled Sanofi
RandomizedParallel-groupDouble-blindPrevention

Summary

The primary objective of the study is to determine whether enoxaparin compared to unfractionated heparin will reduce the composite endpoint of all-cause mortality and non-fatal myocardial re-infarction within 30 days after randomization in patients with acute ST-segment elevation myocardial infarction who are eligible to receive fibrinolytic therapy

Timeline

Start
2002-10
Primary completion
2006-12
Completion
2006-12

Outcome

Met primary endpoint

paper The primary end point occurred in 12.0 percent of patients in the unfractionated heparin group and 9.9 percent of those in the enoxaparin group PMID 16537665 ↗

paper 17 percent reduction in relative risk, P<0.001 PMID 16537665 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Enoxaparin sodium Other / unclassified — —