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Hyperlipidemias clinical trials

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NCT ID: NCT01569867 Completed - Clinical trials for Hypercholesterolemia

Genetic Influences on Statin Blood Concentrations in African Americans

Start date: March 2012
Phase:
Study type: Observational

This study intends to determine the effects of genetic polymorphisms on statin response and daily systemic exposure (24-hour area under the time-concentration curve) of statins in African-American patients.

NCT ID: NCT01569854 Withdrawn - Clinical trials for Hypercholesterolemia

Genetic Influence on Statin Pharmacodynamics

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

The study intends to investigate whether genetics influence how individuals respond to statins (clinical outcomes and changes in carotid intimal media thickness)

NCT ID: NCT01564875 Active, not recruiting - Clinical trials for Chronic Kidney Disease

Efficacy and Safety of Simvast Controlled Release (CR) and Zocor in Chronic Kidney Disease(CKD) Stage 3, 4 and 5 Patients With Hyperlipidemia

HM-SIM4
Start date: December 2010
Phase: Phase 4
Study type: Interventional

Study design - Multicenter, double-dummy, double-blinded, randomized, Phase 4 study - Patients will be randomized to either a study group or a control group in a 1:1 ratio, and will be orally administered the assigned drugs Study Objective -The study is designed to demonstrate that efficacy and safety of morning dosing of Simvast Controlled Release (CR) Tab is not inferior to evening dosing of Zocor Tab in patients with stage 3,4,5 chronic kidney disease with hyperlipidemia Primary objective -to assess the percent change of LDL-C at Week 8 from baseline in Chronic Kidney Disease(CKD) stage 3,4,5 with hyperlipidemia subjects.

NCT ID: NCT01562080 Completed - Hyperlipidemia Clinical Trials

Combined Effects of Bioactive Compounds in Lipid Profile

ARM-PLUS-LDL
Start date: January 2012
Phase: Phase 2/Phase 3
Study type: Interventional

The aim of this study is to demonstrate whether, along with dietary recommendations, Armolipid Plus ® can improve the profile of patients with elevated plasma LDL-C acting as a change of lifestyle therapy (TLC) according to the definition of Adult Treatment Panel III (ATP III)

NCT ID: NCT01550432 Completed - Obesity Clinical Trials

Effects of Glutathione (an Antioxidant) and N-Acetylcysteine on Inflammation

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

The rationale for the potential role of antioxidants in the prevention of cardiovascular diseases (CVD) remains strong despite the disappointing results of recent trials with a few select antioxidant vitamins. Glutathione (GSH) is one of the body's most powerful antioxidant agents but there is a surprising paucity of data on its use as an interventional therapy. Glutathione, when taken orally, is immediately broken down into its constituent amino acids, of which cysteine is the only one to be essential. Available cysteine is the critical determinant of intracellular GSH concentrations. N-acetyl cysteine (NAC) is an antioxidant supplement that has been used to provide a source of cysteine to replete GSH levels. By replenishing endogenous glutathione, it is possible that NAC would exert the same effect(s) as exogenous GSH. However, there is a new delivery system, liposomal GSH, which keeps glutathione intact. In this study, the investigators propose to match the cysteine content of NAC and GSH and compare the effects of these two supplements, at two different doses, on markers of inflammation and oxidative stress.

NCT ID: NCT01541943 Completed - Hyperlipidemia Clinical Trials

Efficacy and Safety of HL-040XC in Essential Hypertension and Hyperlipidemia

Start date: March 2012
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate efficacy and safety of HL-040XC in patients with essential hypertension and hyperlipidemia

NCT ID: NCT01524289 Completed - Clinical trials for Hypercholesterolemia, Familial

Study to Assess the Tolerability and Efficacy of Anacetrapib (MK-0859) Co-Administered With Statin in Participants With Heterozygous Familial Hypercholesterolemia (MK-0859-020)

REALIZE
Start date: February 3, 2012
Phase: Phase 3
Study type: Interventional

The objective of this study is to evaluate the efficacy and tolerability of adding anacetrapib to ongoing statin therapy in participants with heterozygous familial hypercholesterolemia (HeFH).

NCT ID: NCT01476436 Completed - Clinical trials for Overweight and Obesity

Low Carbohydrate Diet - Effect on Plasma Lipids and Metabolic Markers

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

Low carbohydrate diet may influence the plasma lipid levels.

NCT ID: NCT01448174 Completed - Metabolic Syndrome Clinical Trials

Salusin-alpha - a New Factor in the Pathogenesis of Lipid Abnormalities in Hemodialysis Patients

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

Hyperlipidemia and atherosclerosis lead to cardiovascular diseases and are an indirect cause of increased death rate in the general population. This association is still more evident in specific subpopulations, like patients with advanced chronic kidney disease (CKD), especially hemodialysis (HD) patients, due to a higher prevalence of lipid disturbances and atherosclerosis compared to the general population. Cardiovascular events in CKD patients are frequently associated with traditional risk factors, including diabetes, male sex, hypertension, dyslipidemia and advanced age. However, these factors failed to fully account for the increased risk of cardiovascular events in CKD. The efforts are made to identify new risk factors that contribute to the development of atherosclerosis and participate in causes of cardiovascular death. In 2003, there were identified peptides designated salusin-alpha and salusin-beta. Development of atherosclerosis may be suppressed by salusin-alpha. Salusin-alpha may have a lipid lowering effect, similar to that of statins. The purpose of this study is to investigate whether 1) salusin-alpha is associated with lipid metabolism of HD patients (without or with metabolic syndrome or type 2 diabetes mellitus), similarly or not like in healthy or obese subjects; 2) treatment with atorvastatin and its effects are associated with changes in plasma salusin-alpha concentration, if so - whether it is dependent on the direct influence of atorvastatin on salusin-alpha or associated with a decrease in serum lipid level; 3) salusin-alpha may predict mortality in HD patients.

NCT ID: NCT01442987 Completed - Hypertension Clinical Trials

Efficacy and Safety of Irbesartan and Atorvastatin in Hypertension and Hyperlipidemia

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

The purpose of this study is to evaluate efficacy and safety of coadministered Irbesartan and Atorvastatin in patients with hypertension and hyperlipidemia.