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Hyperlipoproteinemias clinical trials

View clinical trials related to Hyperlipoproteinemias.

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NCT ID: NCT00092573 Completed - Clinical trials for Hypercholesterolemia

Study of Ezetimibe and Fenofibrate in Patients With Mixed Hyperlipidemia (0653-036)(COMPLETED)

Start date: April 2003
Phase: Phase 3
Study type: Interventional

The purpose of this study is to assess the cholesterol lowering safety and effectiveness of two investigational drugs in patients with mixed hyperlipidemia (high cholesterol and high triglycerides).

NCT ID: NCT00092560 Completed - Clinical trials for Hypercholesterolemia

Two Investigational Drugs in Patients With Mixed Hyperlipidemia (0653-036)

Start date: December 2002
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the cholesterol lowering effectiveness and safety of two investigational drugs in patients with mixed hyperlipidemia (high cholesterol and high triglycerides).

NCT ID: NCT00059254 Completed - Obesity Clinical Trials

Differential Metabolism of Dietary Fatty Acids

Start date: September 2000
Phase: N/A
Study type: Interventional

Differences in how diet fats are converted to energy could explain some of the reported differences in health effects among different classes of dietary fat (e.g. monounsaturated vs. saturated). Recently, this laboratory showed that monounsaturated fats are turned into energy more readily than saturated fats. These results may mean that if one feeds more monounsaturated fatty acids (MUFA) and less saturated fatty acids (SFA) in the diet, body fat might accumulate at a lower rate. This could affect the risk of obesity and Type 2 Diabetes. This project has two principal Specific Aims which will be assessed in healthy young adults who are fed liquid formulas containing either an approximately equal amount of MUFA and SFA (controls) or a much greater amount of MUFA and much less SFA: 1. To determine if a higher intake of MUFA and a reciprocally lower intake of SFA is associated with a higher rate of fat oxidation. We hypothesize that the rate of fat oxidation after eating will be higher in those subjects randomized to the MUFA-enriched diet compared to controls. 2. To measure energy intake required to maintain constant body weight during each diet and to measure fat-free mass and fat mass, before and after each dietary change. We hypothesize that those on the high MUFA diet will need a higher energy intake required to maintain constant body weight.

NCT ID: NCT00005368 Completed - Clinical trials for Cardiovascular Diseases

Genetic Epidemiology of Hypertriglyceridemia

Start date: July 1993
Phase: N/A
Study type: Observational

To determine prospectively the role of elevated plasma triglyceride (TG) as a risk factor for 20-year coronary heart disease (CHD) mortality in familial combined hyperlipidemia (FCHL) and familial hypertriglyceridemia (FHTG), the familial forms of hypertriglyceridemia. Also, to perform genetic epidemiologic studies of recently identified lipoprotein risk factors for CHD, including Atherogenic Lipoprotein Phenotypes (ALP) based on subclasses of low-density lipoproteins (LDL), Lipoprotein(a) (Lp(a)) and apolipoprotein (apo) B plasma levels, and apo E isoforms.

NCT ID: NCT00005128 Completed - Clinical trials for Cardiovascular Diseases

Lipid Research Clinics Population Studies

Start date: July 1972
Phase: N/A
Study type: Observational

To conduct epidemiologic surveys of the distribution, causes, and consequences of the dyslipoproteinemias. The Population Studies include the Prevalence Study, the Family Study, and the Mortality Follow-up Study and shared the same general population base.

NCT ID: NCT00004466 Terminated - Hyperlipidemia Clinical Trials

Pilot Study of Atorvastatin in Children With Chronic Hyperlipidemia Secondary to Nephrotic Syndrome

Start date: October 1998
Phase: Phase 2
Study type: Interventional

OBJECTIVES: I. Determine the effect of atorvastatin on the plasma levels of lipids, Lp(a), and apoproteins for treating hyperlipidemia in children with nephrotic syndrome in whom proteinuria and hyperlipidemia persist after other appropriate measures to treat their primary disease have been exhausted. II. Determine the safety and tolerability of atorvastatin in these patients. III. Provide preliminary data for a future investigation into the potential effect that lowering cholesterol levels may have on the rate of progression of renal insufficiency in such patients.

NCT ID: NCT00001226 Completed - Healthy Clinical Trials

Lipoprotein Metabolism in Normal Volunteers and Patients With Abnormal Levels of Lipoproteins

Start date: December 1987
Phase: N/A
Study type: Observational

Researchers plan to study the fat-rich particles, called lipoproteins, which circulate in the blood. This study is designed to improve understanding of normal, as well as abnormal, lipoprotein metabolism and the role it plays in the development of hardening of the arteries (atherosclerosis). Patients participating in this study will receive an intravenous (directly into the vein) injection of a small amount of specially prepared amino acids. The amino acids being injected are the same amino acids present in a normal diet. The amount of amino acid given will be less than the amount eaten in a protein-rich meal. The amino acids will be labeled with nonradioactive heavy isotopes which are also present in the environment n low amounts. Patients participating in the study will be required to have blood samples taken, and provide urine samples throughout the course of the study. In addition, patient will be required to follow a specially formulated diet. Patients will be weighed throughout the course of the study.

NCT ID: NCT00000538 Completed - Clinical trials for Cardiovascular Diseases

Dietary Effects on Lipoproteins and Thrombogenic Activity

DELTA
Start date: September 1992
Phase: Phase 3
Study type: Interventional

To evaluate the effects of carefully controlled diets on lipoproteins and clotting factors in different demographic groups.