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Effect of Atorvastatin Administration Before Primary Percutaneous Coronary Intervention

Effect of Atorvastatin Administration Before Primary Percutaneous Coronary Intervention in Patients With ST-segment Elevation Myocardial Infarction

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00610870
Enrollment
173
Registered
2008-02-08
Start date
2007-07-31
Completion date
2009-08-31
Last updated
2011-03-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Angioplasty, Transluminal, Percutaneous Coronary

Keywords

Myocardial infarct size, Atorvastatin, SPECT, Hydroxymethylglutaryl-CoA Reductase Inhibitors

Brief summary

The purpose of this study to determine whether statin pretreatment decrease myocardial infarct size in patients with acute myocardial infarction undergoing primary percutaneous coronary intervention.

Interventions

DRUGatorvastatin

atorvastatin 80mg/day before primary coronary intervention

Sponsors

Samsung Medical Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Presence of chest pain for more than 30 minutes but less than 12 hours after symptom onset * ST segment elevation more than 1 mm in two or more contiguous leads or presumably a new onset left bundle branch blockage

Exclusion criteria

* Cardiogenic shock * History of myocardial infarction * Chronic liver disease * Previous or current statin use

Design outcomes

Primary

MeasureTime frame
Myocardial infarct size by SPECTbetween 5 and 14 days after acute myocardial infarction

Secondary

MeasureTime frame
Myocardial infarct size measured by contrast-enhanced MRIwithin 14 days after acute myocardial infarction
Myocardial blush grade after the procedureimmediate after procedure
complete ST resolutionat 60 minutes after the procedure
major adverse cardiac events related to left ventricular dysfunction (death, new-onset sustained hypotension or heart failure, and hospital readmission for left ventricular dysfunction)at 6 months after the procedure

Countries

South Korea

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026