Clinical Trials Logo

Dyslipidemia clinical trials

View clinical trials related to Dyslipidemia.

Filter by:

NCT ID: NCT00680017 Completed - Dyslipidemia Clinical Trials

30 Week Study of the Combination of ABT-335 and Rosuvastatin Compared to Rosuvastatin Monotherapy for Subjects With Dyslipidemia and Stage 3 Chronic Kidney Disease

Start date: June 2008
Phase: Phase 3
Study type: Interventional

The objective of this study is to evaluate the safety and efficacy of the combination of ABT-335 plus rosuvastatin in dyslipidemic subjects with Chronic Kidney Disease (CKD) Stage 3.

NCT ID: NCT00673881 Completed - Dyslipidemia Clinical Trials

ABT-335 (Choline Fenofibrate) Reverse Cholesterol Transport (RCT) Study

Start date: March 2008
Phase: Phase 1/Phase 2
Study type: Interventional

The objectives of the study are: 1. To evaluate the effect of ABT-335 (choline fenofibrate) on several parameters of RCT (reverse cholesterol transport) in men and post-menopausal women diagnosed with dyslipidemia (i.e., low high-density lipoprotein [HDL] cholesterol levels and elevated triglyceride [TG] concentrations). 2. To evaluate longitudinal changes in several parameters of RCT in subjects with low HDL. 3. To obtain pilot data for power calculations for subsequent comparative study.

NCT ID: NCT00673660 Completed - Dyslipidemia Clinical Trials

Observational Study On Compliance Of Statin Treatment Of Patients With High Blood Cholesterol Levels

Start date: October 2007
Phase:
Study type: Observational

The purpose of the study is to show the compliance rates of the patients to statin treatment and the reasons of non-compliance.

NCT ID: NCT00666250 Completed - Hypertension Clinical Trials

Effects of Xoçai Antioxidant Supplements on Atherosclerosis Risk Factors

Start date: January 2006
Phase: N/A
Study type: Interventional

An antioxidant dietary supplement made from cocoa powder, and extracts of acai, grape and blueberry will be tested for effects on blood sugar, blood pressure, cholesterol and related parameters in human subjects.

NCT ID: NCT00666172 Completed - Obesity Clinical Trials

Effects of Worksite Wellness Interventions on Vascular Function, Insulin Sensitivity and High-Density Lipoprotein in Overweight or Obese Women

Start date: April 8, 2008
Phase: Phase 2
Study type: Interventional

Employees in developed societies are becoming increasingly sedentary at work and at home due to technological advances. Physical inactivity coupled with excess intake of calorie-rich foods are responsible for the epidemic of obesity. In population cohorts, physical inactivity and obesity increase the risk of cardiovascular disease and death. Because of the impact on productivity and health care costs, many businesses and other organizations have initiated "wellness" programs, often with facilities at the work site to encourage exercise. Although these programs have often resulted in improved fitness for participants, weight loss has been more difficult to achieve. In this regard, in our initial study of NIH employees participating in NHLBI's Keep the Beat program--two-thirds of whom were overweight or obese--we found improved exercise fitness after 3 months of participation, with exercise averaging 20 minutes each work day, but no significant weight loss. Associated with greater fitness in our participants was improvement in endothelial function, an important biomarker of cardiovascular risk. Because level of fitness is a strong predictor of cardiovascular (and total) mortality in population studies, some investigators and thought leaders have proposed that it is acceptable to be "fat and fit." We found in our study, however, that exercise alone has little effect on insulin sensitivity and other biomarkers of risk, including C-reactive protein, which could limit further improvement in endothelial function and even greater risk reduction. We propose to test in this protocol whether weight loss through supervised nutritional counseling and daily exercise at worksite facilities confers health benefits beyond those achieved with improved fitness alone, such as improvement in endothelial function, arterial compliance, insulin sensitivity, markers of inflammation in blood and high-density lipoprotein (HDL) structure and function. Because obesity in a sedentary workforce environment is especially prevalent among women, with additional contribution of menopause to obesity, our study will be restricted to overweight and obese women to allow appropriate analysis in a cohort of manageable size for our testing resources. The primary endpoint will be differential improvement in endothelial function, as determined by brachial artery reactivity to shear stress, from baseline to 6 months in participants randomized to exercise coupled with weight-loss intervention versus subjects randomized to exercise alone. Secondary analyses will include comparisons of adiposity, arterial stiffness, insulin sensitivity, HDL subparticles and function, and markers of inflammation and adipokines in blood, with exploratory analyses of minorities and age/hormonal interactions. Demonstration of improved vascular function and other biomarkers of cardiovascular risk with improved fitness combined with weight loss may serve as an incentive for greater participation in organization-initiated wellness programs with emphasis both on exercise and on personalized nutritional counseling.

NCT ID: NCT00665834 Completed - Dyslipidemia Clinical Trials

Comparison of Rosuvastatin and Atorvastatin in Patients With Acute Coronary Syndrome

Start date: April 2006
Phase: Phase 4
Study type: Interventional

This is a 3-month, randomized, parallel-group study with 2 periods, comparing the efficacy and the safety of rosuvastatin 20 mg versus atorvastatin 80 mg in patients with an acute coronary syndrome (ACS).

NCT ID: NCT00664859 Completed - Dyslipidemia Clinical Trials

12-Month, Open-Label, Extension Study of LCP-AtorFen in Dyslipidemia

Start date: October 2007
Phase: Phase 2/Phase 3
Study type: Interventional

The current study is designed to test the long-term (12-month) safety and efficacy of LCP-AtorFen, a combination of atorvastatin and fenofibrate, in patients with dyslipidemia

NCT ID: NCT00664287 Withdrawn - Dyslipidemia Clinical Trials

Extended Release (ER) Niacin/Laropiprant Add on Study (0524A-082)

Start date: September 2008
Phase: Phase 3
Study type: Interventional

The purpose of this study is to test the effect of MK0524A (niacin (+) laropiprant) on lowering bad cholesterol and raising good cholesterol.

NCT ID: NCT00645775 Completed - Obesity Clinical Trials

Effect of Irvingia Gabonensis (Bush Mango)on Parameters Associated With Metabolic Syndrome

Start date: November 2006
Phase: N/A
Study type: Interventional

The study investigated the use and efficacy of the seeds of African bush mango (Irvingia gabonensis)to control body weight, blood lipids and hormones in overweight and obese people.

NCT ID: NCT00634673 Completed - Clinical trials for Type 2 Diabetes Mellitus

Postprandial Fatty Acids and FABP2 in Type 2 Diabetes Mellitus (DM)

Start date: June 2006
Phase: N/A
Study type: Interventional

This study will be conducted in type 2 diabetic patient's to evaluate the if there is a different response of serum lipids after a standard meal (rich in saturated fatty acids) in patients who have the presence of a genetic alteration. This alteration that will be evaluated is a polymorphism, change of an amino acid in the gene of FABP2. This gene that can influence the absorption of lipids in the intestine and subjects who have the altered genotype (presence of T allele) can have an abnormal lipid profile as compared to subjects without this genotype.