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Hyperlipoproteinemia clinical trials

View clinical trials related to Hyperlipoproteinemia.

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NCT ID: NCT02933138 Completed - Clinical trials for Hyperlipoproteinemia

Plasma Triglyceride Lipolysis in Multifactorial Chylomicronemia

Start date: July 2010
Phase: N/A
Study type: Observational

Purpose: The mechanism of most of the multifactorial chylomicronemia (MCM) remains elusive. In order to decipher the mechanisms involved in the occurrence of this disease, plasma TG lipolysis characteristics will be monitored for 60 minutes after heparin injection instead of the 10 minutes gold standard, in a large group of genotyped MCM patients.

NCT ID: NCT01878227 Completed - Clinical trials for Hyperlipoproteinemia

Comparison of Coenzyme A and Fenofibrate for Safety and Efficacy On Patients With Hyperlipidemia

Start date: July 2010
Phase: Phase 3
Study type: Interventional

The purpose of this study is to compare the lipid lowering effects and clinical safety of a natural hypolipidemic compound, coenzyme A capsule with a marketed drug, fenofibrate, in Chinese patients with moderate dyslipidemia.

NCT ID: NCT01811082 Completed - Clinical trials for Hyperlipoproteinemia

Comparison of Coenzyme A and Pantethine Capsule for Safety and Efficacy On Patients With Hyperlipidemia

Start date: July 2010
Phase: Phase 3
Study type: Interventional

The purpose of this study is to compare the lipid lowering effects and clinical safety of a natural hypolipidemic compound, coenzyme A capsule with a marketed drug, Pantethine Capsule, in Chinese patients with moderate dyslipidemia.

NCT ID: NCT01645046 Completed - Clinical trials for Hyperlipoproteinemia

The Effects of Coenzyme A on Serum Lipids in Patients With Hyperlipidemia

Start date: October 2008
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the lipid lowering effects and clinical safety of a natural hypolipidemic compound, coenzyme A (CoA) capsule in Chinese patients with moderate dyslipidemia.

NCT ID: NCT01146522 Completed - Clinical trials for Hyperlipoproteinemia

Safety, Tolerability,Pharmacokinetics(PK)and Pharmacodynamics(PD)Assessment of LCQ908 in Patients With Severe Hypertriglyceridemia

Start date: May 2010
Phase: Phase 1/Phase 2
Study type: Interventional

This study will assess safety, tolerability, and effect of LCQ908 on blood lipids in patients with severe hypertriglyceridemia.

NCT ID: NCT01057654 Completed - Clinical trials for Hypercholesterolemia

A Study Comparing the Mechanisms of Action of Lifibrol and Pravastatin

Start date: January 1996
Phase: Phase 3
Study type: Interventional

Lifibrol is a new lipid-lowering drug which lowers cholesterol to an extent in the order of magnitude of the statins. The mechanism of action of this compound is different from the one of statins but remains unknown. The current study will investigate the mechanism of action using stable-isotope turnover methods. The study will be done in healthy male volunteers.

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: 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.