Metabolic Syndrome Clinical Trial
Official title:
Other Effects of Fluvastatin Are Investigated in Patients With Metabolic Syndrome
Verified date | February 2017 |
Source | Novartis |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Other effects of fluvastatin are investigated in German patients with metabolic syndrome.
Status | Completed |
Enrollment | 55 |
Est. completion date | February 2006 |
Est. primary completion date | February 2006 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 75 Years |
Eligibility |
Inclusion Criteria: - Written informed consent - Male and female patients, aged between 18 and 75 years - Metabolic syndrome according to National Cholesterol Education Program Adult Treatment Panel III (NCEP ATPIII) Exclusion Criteria: - History of heart failure - HIV positive - Stroke Other protocol defined inclusion and exclusion criteria may apply. |
Country | Name | City | State |
---|---|---|---|
Germany | Novartis | Nürnberg |
Lead Sponsor | Collaborator |
---|---|
Novartis |
Germany,
Westphal S, Abletshauser C, Luley C. Fluvastatin treatment and withdrawal: effects on endothelial function. Angiology. 2008 Oct-Nov;59(5):613-8. doi: 10.1177/0003319708316005. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change from baseline in circulating marker of inflammation (C-reactive protein) after 5 weeks | |||
Secondary | Change from baseline in low density lipoprotein cholesterol after 5 weeks | |||
Secondary | Change from baseline in non high density lipoprotein cholesterol after 5 weeks | |||
Secondary | Change from baseline in total cholesterol after 5 weeks | |||
Secondary | Change from baseline in high density lipoprotein cholesterol after 5 weeks | |||
Secondary | Change from baseline in oxidized low density lipoprotein cholesterol after 5 weeks |
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