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Hypercholesterolemia clinical trials

View clinical trials related to Hypercholesterolemia.

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NCT ID: NCT01709513 Completed - Clinical trials for Hypercholesterolemia

Study of Alirocumab (REGN727/SAR236553) in Patients With Primary Hypercholesterolemia and Moderate, High, or Very High Cardiovascular (CV) Risk, Who Are Intolerant to Statins (ODYSSEY ALTERNATIVE)

Start date: September 30, 2012
Phase: Phase 3
Study type: Interventional

This is a randomized, double-blind, double-dummy, active-controlled, parallel-group, multi-national, multi-center study to compare alirocumab (REGN727/SAR236553) versus ezetimibe in participants with primary hypercholesterolemia and moderate, high, or very high CV risk, who are intolerant to statins. An atorvastatin arm is added to determine that the population selected in the study is a truly statin intolerant population by assessing skeletal muscle-related adverse events.

NCT ID: NCT01709500 Completed - Clinical trials for Heterozygous Familial Hypercholesterolemia

Study of Alirocumab (REGN727/SAR236553) in Patients With heFH (Heterozygous Familial Hypercholesterolemia) Who Are Not Adequately Controlled With Their LMT (Lipid-Modifying Therapy)

ODYSSEY FH II
Start date: December 2012
Phase: Phase 3
Study type: Interventional

This is a randomized, double-blind, placebo-controlled, parallel-group, multi-national study alirocumab (REGN727/SAR236553) in patients with Heterozygous Familial Hypercholesterolemia (heFH) who are not adequately controlled with their Lipid-Modifying Therapy (LMT).

NCT ID: NCT01702987 Completed - Clinical trials for Hypercholesterolemia

Evaluation of Ubiquinol on Mitochondrial Oxidative Capacity in Statin Patients Using 31PMRS

Start date: October 2012
Phase: N/A
Study type: Interventional

It is our primary hypothesis that statin drugs impair skeletal muscle mitochondrial function and that ubiquinol (the reduced active form of CoQ10) supplementation will block impairment of PCr recovery kinetics in patients using statins. The investigators propose a pilot study to extend our research to examine PCr recovery kinetics in 20 statin users randomized in a parallel arm study to either ubiquinol or placebo over 4 weeks.

NCT ID: NCT01678521 Completed - Clinical trials for Hypercholesterolemia

Effect of LDL-apheresis on PTX3 Plasma Levels in Hypercholesterolemic Patients

Start date: September 2012
Phase: N/A
Study type: Observational

Inflammation plays a major role in atherosclerosis. Pentraxin 3 (PTX3) a multifunctional pattern-recognition protein, is expressed in many tissues/cells, including innate immunity cells, endothelium and atherosclerotic plaques. Its role is controversial: it may exert protective cardiovascular effects and/or it may be an indicator of plaque vulnerability and future cardiovascular risk. LDL-Apheresis removes apoB100-containing lipoproteins and it can prevent progression of coronary artery disease (CAD). LDL-Apheresis exerts non-lipidic beneficial effects on the procoagulatory state and on hemorheology. No data exist about the effects of LDL-Apheresis on plasma PTX3 levels.

NCT ID: NCT01671085 Completed - Healthy Volunteers Clinical Trials

A Study of LY3015014 in Healthy Participants With High Cholesterol

Start date: August 2012
Phase: Phase 1
Study type: Interventional

This is a study in healthy participants with high levels of "bad" cholesterol who are already taking a popular type of cholesterol-lowering medication called statins. Following multiple doses of LY3015014, investigators will study the safety and tolerability of the drug, how the body handles the drug, and the drug's effect on the body. Participants will remain in the study for about 3 months, not including screening. Screening is required within 28 days before the study starts.

NCT ID: NCT01670734 Completed - Clinical trials for Hypercholesterolemia

Pharmacokinetic and Tolerability of Alirocumab SAR236553 (REGN727) in Patients With Hepatic Impairment and in Healthy Subjects

Start date: September 2012
Phase: Phase 1
Study type: Interventional

Primary Objective: Study the effect of mild or moderate hepatic impairment on the pharmacokinetics of alirocumab SAR236553 (REGN727). Secondary Objectives: - Assess the safety and tolerability of alirocumab SAR236553 (REGN727) in patients with mild and moderate hepatic impairment and in matched subjects with normal hepatic function. - Assess the pharmacodynamic profile of alirocumab SAR236553 (REGN727) in patients with hepatic impairment and in matched subjects with normal hepatic function.

NCT ID: NCT01666067 Completed - Clinical trials for Hypercholesterolemia

Vascular and Metabolic Effects of Vytorin vs Simvastatin

Start date: November 2011
Phase: Phase 4
Study type: Interventional

The investigators hypothesize that vytorin will improve insulin resistance compared with simvastatin

NCT ID: NCT01661543 Completed - Clinical trials for Hypercholesterolemia

U of A/ U of M Beans and Peas Health Claim Project

Start date: January 2013
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to compare how regularly eating (dried) beans or peas or rice (control) lowers blood lipids, particularly Low Density Lipoprotein cholesterol and total cholesterol, in mildly hypercholesterolemic men and women. The investigators hypothesize that regularly eating beans or peas will significantly improve blood lipid profiles in these people. Participants in this study will consume 1 study food item 5 out of 7 days a week containing beans or peas or rice for a total of 6 weeks. This study will benefit Canadian pulse growers by enhancing development of food products for human consumption and supporting marketing strategies to increase awareness that a diet rich in pulses can improve human health. Measuring changes in blood and urinary polyphenol levels will help to verify whether these compounds play a role in the beneficial actions of beans and peas and subsequently assist with the identification of the beneficial bean/pea components. This in turn, will enable crop breeders to select for plants that are rich in these compounds.

NCT ID: NCT01660945 Completed - Clinical trials for Hypercholesterolemia

Vascular and Metabolic Effects of Vytorin

Start date: July 2011
Phase: Phase 4
Study type: Interventional

The investigator hypothesize that vytorin may improve vascular and insulin resistance in hypercholesterolemic patients

NCT ID: NCT01660919 Completed - Clinical trials for Hypercholesterolemia

Vascular and Metabolic Effects of Rosuvastatin

Start date: October 2011
Phase: Phase 4
Study type: Interventional

The investigators hypothesize that rosuvastatin does-dependently worsens insulin sensitivity.