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Dyslipidemias clinical trials

View clinical trials related to Dyslipidemias.

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NCT ID: NCT00945217 Recruiting - Dyslipidemia Clinical Trials

The Roles of SAH Gene Family in Athrogenic Dyslipidemia in Postmenopausal Women

MOSAH-S2
Start date: October 2009
Phase: N/A
Study type: Observational

Atherogenic dyslipidemia is characterized by high levels of apolipoprotein B (apoB)-containing lipoproteins, including very-low-density lipoprotein (VLDL) and its remnants and small, dense LDL (sdLDL) particles, and reduced levels of high-density lipoprotein cholesterol (HDL-C). The National Cholesterol Education Program (NCEP) recommended using non-high-density lipoprotein cholesterol (non-HDL-C) to surrogate atherogenic lipoproteins in clinical practice. Recently, the investigators have done a pilot study to study the associations between SAH gene variants and atherogenic dyslipidemia (surrogated by non-HDL-C) in postmenopausal women. The investigators found that homozygosity for SAH haplotype 3 was associated with increased adiposity, insulin resistance, and elevated levels of non-HDL-C in the postmenopausal women. Based on the findings of the pilot study, the investigators plan to expand the cohort of postmenopausal women to about 800 women, that is, recruited 660 new subjects in two years. The associations between non-HDL-C and the SAH gene family will be done. Fasting blood sampling for buffy coats and lipids is the core test of Study 2. A 75-g oral glucose tolerance test (OGTT) will be available as an optional test for a better phenotyping of insulin resistance for the participants. Detailed lipid profiling including measurements of VLDL cholesterol, VLDL-TG, remnant lipoprotein, LDL particle size, apoA1, apoB, and apoCIII will be done in the second year of the study if significant associations between gene variants of the SAH gene family and non-HDL-C are detected.

NCT ID: NCT00944645 Completed - Dyslipidemia Clinical Trials

MK0524A Bioequivalence Study (0524A-059)

Start date: October 2006
Phase: Phase 1
Study type: Interventional

This study will evaluate the definitive bioequivalence of tablets of MK0524A (1000 mg Extended Release (ER) Niacin/ 20 mg laropiprant) from two sources.

NCT ID: NCT00943124 Completed - Dyslipidemia Clinical Trials

MK0524B Bioequivalence Study (0524B-070)

Start date: July 2007
Phase: Phase 1
Study type: Interventional

This study will evaluate: 1. the bioequivalence of simvastatin and simvastatin acid following dose of simvastatin (ZOCORâ„¢) given together with one tablet of MK0524A or as a component of the triple combination tablet MK0524B. 2. the bioequivalence of laropiprant and ER niacin when administered as the triple combination tablet MK0524B or as the double combination tablet MK0524A given together with simvastatin.

NCT ID: NCT00935259 Completed - Clinical trials for Hypercholesterolemia, Dyslipidemia

Lipid Biomarker Study in Men With Dyslipidemia After Simvastatin Treatment (Study MK-0000-140)(COMPLETED)

Start date: July 2009
Phase: Phase 1
Study type: Interventional

The purpose of this study was to provide human lipidomics standards with simvastatin treatment that were to be used for comparison with similar preclinical studies.

NCT ID: NCT00934908 Withdrawn - Schizophrenia Clinical Trials

Prevention of Weight Gain and Dyslipidemia by Green Tea in Patients Initiating Therapy With Olanzapine

Start date: March 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if taking green tea capsules can help prevent weight gain in patients that start therapy with Zyprexa® (olanzapine).

NCT ID: NCT00933647 Recruiting - Obesity Clinical Trials

Cardioprotective Effects of Green Tea Versus Maté Intake

Start date: November 2007
Phase: Phase 3
Study type: Interventional

The investigators aim to study the effects of green tea and maté consumption on lipid and inflammatory profiles in dyslipidemic and overweight subjects.

NCT ID: NCT00931320 Completed - Dyslipidemias Clinical Trials

Investigation Into the RAtio of LDL-CHolestEroL to HDL-Cholesterol Improvement After Statin Treatment in Korean Patients

RACHEL
Start date: July 2009
Phase: N/A
Study type: Observational

An observational, non-interventional, multi-centre study to provide further information on the ratio of LDL-C to HDL-C improvement after statin treatment in Korean patients group.

NCT ID: NCT00928694 Completed - Dyslipidemia Clinical Trials

Fenofibrate Bioequivalence Study (0767-031)

Start date: February 2003
Phase: Phase 1
Study type: Interventional

This study will determine definitive bioequivalence of the United States (U.S.) and United Kingdom (UK) formulations of fenofibrate following administration of single doses in healthy adult subjects.

NCT ID: NCT00926744 Active, not recruiting - Hypertension Clinical Trials

Nutrition and Exercise Intervention Study

NEXIS
Start date: April 2006
Phase: N/A
Study type: Interventional

The purpose of the present study was to clarify the effects of increase in physical activity on incidence and surrogate marker of cardiovascular diseases. The working hypothesis of the present study was that the physical activity to satisfy the Japanese guideline of Ministry of Health, Labour and Welfare is effective for the primary prevention of the lifestyle-related disease.

NCT ID: NCT00911482 Completed - Clinical trials for Diabetes Mellitus, Type 2

Production of Free Fatty Acids From Blood Triglycerides

Start date: June 2008
Phase: N/A
Study type: Observational

The overall hypothesis of these studies is that circulating triglycerides, coming primarily from fat in the diet, are an important source of free fatty acids. Free fatty acids are the major fat fuel in the body, and when they are elevated in the blood they are thought to raise the risk of cardiovascular disease by causing insulin resistance (in some cases leading to diabetes), raising blood pressure, and other effects. The investigator will use sophisticated methods for tracing triglycerides and free fatty acids in the blood. These methods involve the administration of low doses of radioactive and stable isotopes of naturally occurring fats. The studies will determine the contribution of triglycerides to free fatty acids in normal people and also in people with diabetes.