drugset / Trial / NCT01936805

ROsuvastatin LOading and Clinical Outcomes Trial

NCT01936805

Phase 3 Completed 299 enrolled Yuksek Ihtisas Hospital
RandomizedParallel-groupDouble-blindTreatment

Summary

The aim of the present study was to evaluate the effect of pre-procedural single high loading dose (40 mg) of rosuvastatin on the primary end-points of all cause mortality and composite of death or myocardial infarction from cardiovascular (CV) causes, target vessel revascularization (TVR), or stroke.

Timeline

Start
2008-01
Primary completion
2012-01
Completion
2012-01

Drugs

EvaluationDrugModalityDoseRoute
Comparator Rosuvastatin Small molecule 40 mg

Indications