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Dyslipidemias clinical trials

View clinical trials related to Dyslipidemias.

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NCT ID: NCT00462046 Completed - Clinical trials for Diabetes Mellitus, Type 2

Efficacy and Safety of Berberine in the Treatment of Diabetes With Dyslipidemia

Start date: April 2005
Phase: Phase 3
Study type: Interventional

Berberine has showed effective in lowering blood sugar levels in db/db mice and anti-dyslipidemia in human. These findings have not been tested in a clinical trial. This randomized, double blind, placebo controlled and multi-center study has demonstrated that berberine is effective in lowering plasma glucose concentrations, reducing serum HbA1c and anti-dyslipidemia in type 2 diabetic patients with dyslipidemia.

NCT ID: NCT00458081 Terminated - Obesity Clinical Trials

Evaluation of the Rimonabant Impact on the Regression of Asymptomatic Damage Caused by Cardiovascular Risk Factors

RIALTO
Start date: March 2007
Phase: Phase 3
Study type: Interventional

Primary objective: - To assess the effect on microalbuminuria levels of treatment with rimonabant 20 mg versus a placebo during a 12 month period. Secondary objectives: - Percentage of patients in both arms of the study whose levels of microalbuminuria decrease, stabilise, increase towards macroalbuminuria or are unchanged after 12 months of treatment with rimonabant or placebo. - To assess the effect of treatment with rimonabant 20 mg versus placebo over a 12 month period on: - Weight and waist circumference. - Glycaemia profile: fasting glycaemia, fasting insulinaemia and HbA1c. - Lipid and lipoprotein profile: triglycerides, total cholesterol, HDL-C, LDL-C, apolipoproteins A1 and B. - Inflammatory markers - Adipocytokines. - Blood pressure. - Glomerular filtration rate. - To assess the quality of life by means of questionnaire filled in. - Safety parameters

NCT ID: NCT00455403 Completed - Hypertension Clinical Trials

Atheroma Reduction With Chloroquine in Patients With the Metabolic Syndrome (ARCH-MS)

ARCH-MS
Start date: April 2006
Phase: N/A
Study type: Interventional

Metabolic syndrome consists of a group of co-occuring conditions that increase an individual's risk of developing heart disease, stroke, and diabetes. The purpose of this study is to evaluate the long-term effectiveness of chloroquine, a protein-activation medication, at reducing the progression of atherosclerosis in patients with the metabolic syndrome. Sub-study: Vascular endothelial growth factor(VEGF)and Cardiometabolic Risk, The purpose is to determine if the association of VEGF with atherosclerosis indicates that it should be a marker of the disorder.

NCT ID: NCT00455325 Completed - Hypertension Clinical Trials

Chloroquine to Treat People With Metabolic Syndrome Aim2 (ARCH-MS)

ARCH-MS
Start date: September 2004
Phase: Phase 2
Study type: Interventional

Metabolic syndrome consists of a group of co-occuring conditions that increase an individual's risk of developing heart disease, stroke, and diabetes. The purpose of this study is to evaluate the short-term effectiveness of chloroquine, a protein-activation medication, at improving metabolic syndrome.

NCT ID: NCT00447070 Completed - HIV Infections Clinical Trials

Effect of Atazanavir on Endothelial Function in HIV-Infected Patients

ENDOPACT
Start date: August 2004
Phase: Phase 4
Study type: Interventional

It is known that certain antiviral therapies, the socalled protease inhibitors, used in the treatment of HIV infection has an untowarded effect on the blood vessels, promoting early occurence of atherosclerosis. A a newer protease inhibitor, atazanavir, has been shown to have no negative effect on the levels of blood cholesterol and it is hypothesized that this may indicate that atazanavir is less prone to induce atherosclerosis. An early sign of atherosclerosis is a reduced vasomotion and this study investigate the influence of atazanavir on functionality of the conduit blood vessels compared to that of "standard" antiviral therapy.

NCT ID: NCT00442845 Completed - Clinical trials for Diabetes Mellitus, Type 2

Establish The Benefits Of Using Various Starting Doses Of Atorvastatin On Achievement Of Cholesterol Targets (ACTFAST)

ACTFAST
Start date: January 2003
Phase: Phase 4
Study type: Interventional

Physicians tend to always use the lowest dose of statins to initiate therapy even in subjects who require large reductions in cholesterol. The study evaluates if selecting the starting dose based on baseline and target LDL-C cholesterol would provide better results (ie proportion of subjects resching target)

NCT ID: NCT00442325 Completed - Clinical trials for Diabetes Mellitus, Type 2

Benefits Of Using Various Starting Doses Of Atorvastatin On Achievement Of Cholesterol Targets

ACTFAST 2
Start date: January 2003
Phase: Phase 4
Study type: Interventional

European physicians tend to always use the lowest dose of statins to initiate therapy even in subjects who require large reductions in cholesterol. The study evaluates if selecting the starting dose based on baseline and target LDL-C cholesterol would provide better results (ie proportion of subjects resching target)

NCT ID: NCT00441480 Completed - Dyslipidemia Clinical Trials

Effect of Plant Sterols Esterified to Fish Oil Fatty Acids on Plasma Lipid Levels

Start date: March 2007
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether plant sterols esterified to fish oil fatty acids in a fish oil matrix improve the lipid profile, predominantly LDL-cholesterol and TG concentrations in healthy hyperlipidemic subjects.

NCT ID: NCT00438061 Completed - Obesity Clinical Trials

Effect of Abdominal Obesity on Lipoprotein Metabolism

Start date: January 1995
Phase: Phase 3
Study type: Interventional

Abdominal obesity is strongly associated with dyslipidemia, which may account for the associated increased risk of atherosclerosis and coronary disease. Weight reduction is suggested to be a preferred and effective first-line strategy to correct lipid abnormalities, particularly in overweight/obese subjects. This improvement may be related to the effect of reduction in abdominal fat mass on apoB and apoA-I metabolism, but this remains to be fully demonstrated. Hypothesis: Reduction in abdominal fat mass by weight loss decreases apoB concentration and raises HDL-cholesterol chiefly by increasing LDL-apoB fractional catabolic rate (FCR), as well as decreasing HDL apoA-I, respectively.

NCT ID: NCT00434096 Terminated - Obesity Clinical Trials

Japanese Study of Rimonabant in Obese Patients With Dyslipidemia (VENUS)

Start date: February 2007
Phase: Phase 3
Study type: Interventional

The primary objective of this study is to assess the efficacy of SR141716 compared to placebo on body weight and triglycerides changes over a period of 52 weeks. Secondary objectives are: - To evaluate the effect of SR141716 compared to placebo over a period of 52 weeks, on HDL-cholesterol and visceral fat area. - To evaluate the safety of SR141716 compared to placebo over a period of 104 weeks. - To evaluate the pharmacokinetics of SR141716.