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Hyperlipidemias clinical trials

View clinical trials related to Hyperlipidemias.

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NCT ID: NCT01360567 Completed - Type 2 Diabetes Clinical Trials

The Effect of Green Tea Extract on Type 2 Diabetes With Hyperlipidemia

Start date: May 2011
Phase: Phase 3
Study type: Interventional

The aim of the study is to examine whether the extract of green tea is effective on type 2 diabetes and hyperlipidemia.

NCT ID: NCT01353404 Completed - Hyperlipidemia Clinical Trials

Relative Bioavailability Study of Lipidil® Supra (Fenofibrate 160mg) Versus SYO-0805 (Fenofibrate 65mg)

Start date: June 2011
Phase: Phase 1
Study type: Interventional

The purpose of this study is to evaluate the bioequivalence of Lipidil® Supra (fenofibrate 160mg) versus SYO-0805 (fenofibrate 65mg) in single dose oral administration.

NCT ID: NCT01349010 Completed - Hyperlipidemia Clinical Trials

Efficacy and Safety of Imported Probucol to Treat Hyperlipidemia

Start date: April 2011
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the efficacy and safety of imported Probucol in hyperlipidemia patients.

NCT ID: NCT01332747 Completed - Hyperlipidemia Clinical Trials

Clinical Study to Evaluate Antihyperlipidemic Effect of a Classical Unani Antiobesity Formulation

Start date: May 2010
Phase: Phase 2
Study type: Interventional

The purpose of this clinical trial is to study the comparative effect of a classical unani antiobesity drug safoof-e-muhazzil on hyperlipidemia in its classical powder form and in compressed tablet form against a standard control.

NCT ID: NCT01327014 Completed - Hyperlipidemia Clinical Trials

Efficacy and Safety Study of Lipid-Lowering Effects of XueZhiKang (XZK) in Patients With Hyperlipidemia

Start date: April 2011
Phase: Phase 2
Study type: Interventional

The purpose of this study is to demonstrate the efficacy of XueZhiKang to improve plasma lipid profile, as compared to placebo, in outpatients with hyperlipidemia.

NCT ID: NCT01326442 Completed - Obesity Clinical Trials

Vitamin D and Omega-3 Inhibit Metabolic Syndrome

Start date: April 2011
Phase: Phase 3
Study type: Interventional

The study will test the hypothesis that supplementing the diet of subjects with Metabolic Syndrome with 2000 IU vitamin D and 1.8 g omega-3 fatty acids (EPA + DHA) per day, will facilitate weight loss, improve body composition and reduce metabolic and biochemical risk factors associated with type II diabetes and cardiovascular disease. Adult men and women who meet the International Diabetes Federation criteria for Metabolic Syndrome will be enrolled and embark on a 16 week diet and exercise intervention using a low glycemic index diet with or without the supplementary vitamin D and omega-3. Subjects will be counseled weekly and blood collected at weeks 0 and 16.

NCT ID: NCT01317524 Completed - Inflammation Clinical Trials

The Effects of Homogenized and Unhomogenized Milk on Postprandial Metabolism in Healthy Overweight Men

Start date: February 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the effects of homogenized, unhomogenized and skimmed milk on postprandial metabolism in healthy overweight men

NCT ID: NCT01308710 Completed - Hyperlipidemia Clinical Trials

The Effects of a Mediterranean Diet in Pediatric Hyperlipidemia

EARLYMedit
Start date: January 2010
Phase: Phase 1
Study type: Interventional

Children with high cholesterol levels are especially vulnerable and are at high risk for early onset coronary heart disease (CHD). Endothelial dysfunction, the earliest phase of CHD, is present in children with elevated cholesterol levels as early as 8 years of age. The long term objective of this study is to develop dietary interventions for the prevention and treatment of endothelial dysfunction in children with common lipid disorders including familial hypercholesterolemia (FH) and familial combined hyperlipidemia (FCH). Increasing evidence suggests that the Mediterranean diet and ω-3 fatty acids found in fish have cardioprotective effects. The specific aims of the study are to: determine whether a Mediterranean diet alone or combined with ω-3 fatty acid (eicosapentaenoic acid)improves endothelial function; evaluate the effects of the dietary interventions on lipids and lipoprotein subclasses; evaluate the effects of the dietary interventions on biomarkers for oxidative stress and inflammation. This study is a randomized, double-blind, placebo-controlled clinical trial that includes 34 children (ages 8-17) treated with the Mediterranean diet and ω-3 fatty acid supplements. A dietary educational behavioral intervention will be conducted over 6 months with individual counseling and group sessions. Endothelial function will be measured noninvasively by high resolution ultrasound of the brachial artery at baseline, 6, 12, 18 and 24 weeks. This study is unique because it is a new intervention designed for children at high risk for early CHD with a dietary component and supplementation with ω-3 fatty acids. If effective, this intervention would be broadly applicable in the community and lend valuable insight about dietary therapy to prevent the progression of CHD in hyperlipidemic children.

NCT ID: NCT01291641 Completed - Hyperlipidemias Clinical Trials

Effect of Probucol and/or Cilostazol on Mean IMT in Patients With Coronary Heart dIsease

IMPACTonIMT
Start date: March 2011
Phase: Phase 4
Study type: Interventional

The purpose of this study is to evaluate the additional effect of probucol or concomitant administration of cilostazol and probucol on mean carotid artery intima-media thickness (mean IMT) at year 1, 2, and 3.

NCT ID: NCT01280604 Completed - Hyperlipidemias Clinical Trials

Effect of Fenofibrate Conversion on Triglyceride Levels in Patients on Statin Therapy

Start date: October 2010
Phase: N/A
Study type: Interventional

The primary objective of this randomized trial is to measure the impact of converting patients on statin therapy from fenofibrate 160mg to 54mg per day compared to patients who continue fenofibrate 160mg per day for triglycerides.