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Sponsored by: |
AstraZeneca |
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Information provided by: | AstraZeneca |
ClinicalTrials.gov Identifier: | NCT00228514 |
At one site, patients participating in the Corona main study are asked to participate in the PET-substudy. Before and 6 months after study medication is started a Positron Emission Tomography (PET-scan) is performed to study the effect of rosuvastatin in Chronic Heart Failure on myocardial perfusion (reserve)
Condition | Intervention | Phase |
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Rosuvastatin Heart Failure Positron Emission Tomography (PET) |
Drug: Rosuvastatin Procedure: Positron emission tomography |
Phase III |
Study Type: | Interventional |
Study Design: | Treatment, Randomized, Double-Blind, Placebo Control, Parallel Assignment, Efficacy Study |
Official Title: | Sub Study: Controlled Rosuvastatin Multinational Study in Heart Failure (CORONA) PET Sub Study |
Estimated Enrollment: | 40 |
Study Start Date: | February 2004 |
Study Completion Date: | July 2007 |
Ages Eligible for Study: | 60 Years and older |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Study ID Numbers: | 4522IL/0098 Dutch SubStudy, D3562C00098 |
Study First Received: | September 27, 2005 |
Last Updated: | June 10, 2009 |
ClinicalTrials.gov Identifier: | NCT00228514 History of Changes |
Health Authority: | Netherlands: Medical Ethics Review Committee (METC) |
Antimetabolites Heart Failure Rosuvastatin Heart Diseases |
Antilipemic Agents Anticholesteremic Agents Hydroxymethylglutaryl-CoA Reductase Inhibitors |
Antimetabolites Heart Failure Rosuvastatin Heart Diseases Molecular Mechanisms of Pharmacological Action Therapeutic Uses |
Antilipemic Agents Enzyme Inhibitors Cardiovascular Diseases Anticholesteremic Agents Hydroxymethylglutaryl-CoA Reductase Inhibitors Pharmacologic Actions |