Status:

COMPLETED

Assessment of the Lipid Lowering Effect of Rosuvastatin Compared to Atorvastatin in Subjects With Coronary Heart Disease

Lead Sponsor:

AstraZeneca

Conditions:

Coronary Heart Disease

Eligibility:

All Genders

18+ years

Phase:

PHASE4

Brief Summary

The purpose of this study is to compare the efficacy between two lipid lowering treatments, rosuvastatin (10-40 mg) and atorvastatin (20-80 mg) in reducing low-density lipoprotein cholesterol (LDL-C) ...

Eligibility Criteria

Inclusion

  • 18 years or older, established coronary heart disease with a previously performed PCI, previous treatment with clopidogrel, ongoing statin treatment, LDL-C\>2.9 mmol/L, signed informed consent.

Exclusion

  • Ongoing treatment with clopidogrel for more than 12 weeks after randomisation, hypersensitivity to any of the study drugs, active liver disease, moderate or severe renal impairment, hereditary for or known muscular or neuromuscular disease and/or increased serum CK, pregnancy or lactation or of childbearing potential not practising an adequate method of contraception, use of concomitant medication with possible interaction with

Key Trial Info

Start Date :

January 1 2004

Trial Type :

INTERVENTIONAL

End Date :

March 1 2006

Estimated Enrollment :

255 Patients enrolled

Trial Details

Trial ID

NCT00235950

Start Date

January 1 2004

End Date

March 1 2006

Last Update

November 19 2010

Active Locations (18)

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Page 1 of 5 (18 locations)

1

Research Site

Danderyd, Sweden

2

Research Site

Eksjö, Sweden

3

Research Site

Falun, Sweden

4

Research Site

Gothenburg, Sweden