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Hyperlipidemias clinical trials

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NCT ID: NCT00640549 Terminated - Clinical trials for Diabetes Mellitus, Type 2

Atorvastatin and LDL Profile in Non-Insulin Dependent Diabetes Mellitus

ALPIN
Start date: March 2003
Phase: Phase 4
Study type: Interventional

The study will investigate the effects of atorvastatin on the concentrations of small, dense LDL and HDL subfractions in patients with diabetes and the underlying mechanisms of these effects.

NCT ID: NCT00525109 Terminated - Hyperlipidemias Clinical Trials

Elevated Serum HDL in Four Generations of a Nashville Family

Start date: June 2004
Phase: N/A
Study type: Observational

The purpose of this study is to determine the genetic basis of one family's hereditary hyper-HDL-emia using multiple modalities such as linkage analysis and gene array.

NCT ID: NCT00525083 Terminated - Hyperlipidemia Clinical Trials

Protein and Phospholipid Analysis of HDL in Patients With Very High Serum Levels of HDL-C

Start date: June 2005
Phase: N/A
Study type: Observational

Coronary heart disease (CHD) is the single leading cause of death in the United States . Serum Cholesterol is known to have a direct impact on a number of human diseases through a variety of mechanisms. This is particularly true of cardiovascular disease. Measurement and manipulation of serum cholesterol has become a primary focus of primary care physicians and cardiologists when attempting to reduce risk of heart disease.

NCT ID: NCT00477191 Terminated - Obesity Clinical Trials

Effects of TNF-alpha Antagonism (Etanercept) in Patients With the Metabolic Syndrome and Psoriasis

Start date: May 2007
Phase: N/A
Study type: Interventional

People with psoriasis have significantly higher rates of obesity, diabetes, heart failure and high blood pressure than the general public. The purpose of this study is to determine how substances produced in the fat (inflammatory markers) relate to the risk of heart disease in people with the metabolic syndrome and psoriasis. People with metabolic syndrome have insulin resistance, increased waist size, high blood pressure, or high cholesterol.

NCT ID: NCT00299169 Terminated - Diabetes Clinical Trials

Randomized Trial Comparing N of 1 Trials to Standard Practice to Improve Adherence to Statins in Patients With Diabetes

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

Patients who are intolerant of statins in routine practice, but who lack objective evidence of significant harm, will be randomized to receive statins by either n of 1 trials or standard practice. Our hypothesis is that n of 1 trials will improve statin adherence, thereby improving low density lipoprotein cholesterol (LDL-C) levels.

NCT ID: NCT00288483 Terminated - Clinical trials for Hypercholesterolemia

Cholesterol-Lowering Effects of Policosanol

Start date: September 2000
Phase: Phase 3
Study type: Interventional

Despite undeniable progress in the reduction of morbidity and mortality of coronary heart disease (CHD) prevention is a mainstay for medical intervention. The importance of elevated serum cholesterol for the formation and progress of CHD can be regarded as proved after the results of the major intervention studies became available. These studies have provided key evidence for a positive correlation of lipid lowering and decreased mortality. Other studies in patients with established CHD have shown that stabilization and regression of atherosclerotic lesions is possible with lowering of cholesterol using a variety of agents. Different studies have also investigated the long-term effects of lipid lowering strategies on atherosclerosis by means of coronary angiography and have demonstrated that lipid reduction reduces progression of atherosclerosis and can promote atherosclerosis regression. Thus, it has been demonstrated that cholesterol lowering therapy reduces the risk of CHD and diminishes cardiovascular morbidity and mortality. Policosanol is a drug that presumably possesses both hypocholesterolemic and antiplatelet effects. Furthermore there are hints to even more positive effects that influence the development of atherosclerosis, i.e. inhibition of LDL peroxidation and smooth muscle cell proliferation. Previous studies showed efficacy in dose ranges of mostly 5 to 20 mg Policosanol per day. As nearly all previous studies have been performed in Latin America it cannot be excluded that either ethnic or nutritional factors contribute to the dose found to be optimal in this region. This circumstance as well as the requirement to meet the ICH Guideline “Ethnic Factors in the Acceptability of Foreign Clinical Data” make further studies, i.e. a dose-finding clinical trial, an efficacy clinical trial in European patients and a long-term tolerability clinical trial in Caucasian patients necessary. It is known from more than 60 clinical studies performed so far that Policosanol has an excellent safety profile. A placebo-controlled design was considered appropriate as patients with two or more risk factors for the development of cardiovascular events and a LDL of greater than 190 mg/dl were excluded; the chance of getting an active lipid-lowering agent during the treatment phase was 80 %.

NCT ID: NCT00267280 Terminated - Clinical trials for Hypercholesterolemia

A Clinical Trial Comparing Torcetrapib/Atorvastatin To Simvastatin In Subjects With High Cholesterol (A5091031).

Start date: January 2006
Phase: Phase 3
Study type: Interventional

The Torcetrapib project was terminated on December 2, 2006 due to safety findings. Cholesterol levels will be measured over six weeks in subjects being treated with two different kinds of cholesterol medications to see how the different treatments compare to one another.

NCT ID: NCT00267267 Terminated - Dyslipidemia Clinical Trials

A Clinical Trial Comparing Torcetrapib/Atorvastatin to Ezetimibe/Simvastatin In Subjects With A Cholesterol Disorder.

Start date: January 2006
Phase: Phase 3
Study type: Interventional

The Torcetrapib project was terminated on December 2, 2006 due to safety findings. Cholesterol levels will be measured over six weeks in subjects being treated with two different kinds of combination cholesterol medications to see how the different treatments compare to one another.

NCT ID: NCT00231621 Terminated - Obesity Clinical Trials

A Study on Efficacy and Safety of Topiramate in Treatment of Obese Subjects With Dyslipidemia

Start date: May 2001
Phase: Phase 3
Study type: Interventional

The purpose of this study is to compare the efficacy and safety of daily topiramate versus placebo for the treatment of obese subjects with dyslipidemia.

NCT ID: NCT00166166 Terminated - Hyperlipidemia Clinical Trials

Endothelial Hyperpolarization in Humans

Start date: July 2002
Phase: Phase 2
Study type: Interventional

The purpose of this study is to elucidate the role Endothelium-Derived Hyperpolarizing Factor (EDHF) plays in dilating blood vessels and whether it differs between healthy people and those with high cholesterol. A second purpose of the study is to determine the identity of EDHF.