Clinical Trials Directory

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UnknownNCT01033058

Intensive Statin Treatment for STEMI Patients Undergoing Primary PCI

Effect of Intensive Statin Treatment on 90-day Prognosis of STEMI Patients Undergoing Emergency Primary PCI Compared With Usual Care

Status
Unknown
Phase
Phase 4
Study type
Interventional
Enrollment
500 (estimated)
Sponsor
Beijing Chao Yang Hospital · Academic / Other
Sex
All
Age
20 Years – 75 Years
Healthy volunteers
Not accepted

Summary

This is a retrospective, randomized, parallel, open-labeled, controlled study to find out whether STEMI patients undergoing emergency PCI can benefit from intensive atorvastatin treatment compared with routine treatment.

Detailed description

ARMYDA-ACS, ARMYDA-RECAPTURE and NAPLES II demonstrated that in patients with ASP and NSTE ACS undergoing early PCI, loading dose of atorvastatin before early PCI led to a reduction of prei-PCI MI, recurrent CV events and mortality. While, theses studies included patients with non-ST-segment elevation ACS, requiring PCI; these results cannot be extrapolated directly to patients with ST-segment elevation MI, and these trials included patients sent to an early and selective PCI, but not those undergoing emergency revascularization; This study is designed to find out whether STEMI patients undergoing emergency PCI can benefit from intensive atorvastatin treatment compared with routine treatment.

Conditions

Interventions

TypeNameDescription
DRUGatorvastatin80mg atorvastatin immediately after enrollment, emergency PCI,atorvastatin 40mg/d and other usual medication after PCI
DRUGatorvastatinNo loading dose of statin after enrollment, emergency PCI, atorvastatin 20mg/d and other usual medication after PCI

Timeline

Start date
2009-12-01
Primary completion
2011-03-01
Completion
2011-06-01
First posted
2009-12-16
Last updated
2009-12-24

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT01033058. Inclusion in this directory is not an endorsement.