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Hypercholesterolemia clinical trials

View clinical trials related to Hypercholesterolemia.

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NCT ID: NCT00378833 Completed - Clinical trials for Hypercholesterolemia

Tolerability of MK0524A Versus Niacin Extended-Release (0524A-054)

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

This is a 16-week clinical trial in lipid clinic patients for whom niacin therapy is appropriate to evaluate the tolerability of MK0524A versus niacin extended-release. There will be 6 scheduled clinic visits and 2 treatment groups.

NCT ID: NCT00376584 Completed - Hyperlipidemia Clinical Trials

Effect of an Investigational Compound on Tolerability of Extended Release Niacin (0524A-023)(COMPLETED)

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

This is a 12-week clinical trial in lipid clinic patients for whom niacin therapy is appropriate to evaluate the efficacy of MK0524 to improve the tolerability of extended-release niacin. There will be 6 scheduled clinic visits and 3 treatment arms.

NCT ID: NCT00363233 Completed - Type 2 Diabetes Clinical Trials

The Potential Effects and Mechanisms of Flax Lignans on Type 2 Diabetes Mellitus

Start date: March 2006
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of the study is to improving the lipid profile and glucose control in type 2 diabetic patients with supplementation of flax lignans. We hypothesize that flax lignans supplement will improve the cholesterol profile and glucose control in type 2 diabetic patients.

NCT ID: NCT00362180 Completed - Clinical trials for Hypercholesterolemia

Measure Liver Fat Content After ISIS 301012 (Mipomersen) Administration

Start date: July 2006
Phase: Phase 2
Study type: Interventional

This study will assess what, if any, effect that ISIS 301012 (mipomersen) has on liver triglyceride content in multiple groups of subjects with varying degrees of risk for hepatic steatosis. In order to enroll subject groups with varying degrees of risk, the study has included multiple cohorts (Cohorts A-G). Additions and removal of cohorts has been accomplished with protocol amendments.

NCT ID: NCT00355615 Completed - Clinical trials for Familial Hypercholesterolemia

PLUTO: Pediatric Lipid-redUction Trial of rOsuvastatin

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

The primary objective of this study is to determine the efficacy of once-daily rosuvastatin in reducing LDL-C in children and adolescents aged 10-17 years with HeFH from baseline (Day 0) to the end of the 12-week double-blind treatment period.

NCT ID: NCT00353782 Recruiting - Atherosclerosis Clinical Trials

Causes and Natural History of Dyslipidemias

Start date: October 14, 2003
Phase:
Study type: Observational

This study will evaluate people with dyslipidemias - disorders that affect the fat content in the blood. Fats, or lipids, such as cholesterol and triglycerides, are carried in the blood in particles called lipoproteins. These particles are involved in causing blood vessel diseases that can lead to conditions like atherosclerosis (hardening of the arteries) or heart attack. Participants will undergo accepted medical tests and procedures to evaluate their condition. Most of the test results are helpful in making a diagnosis and in guiding treatment. People with lipid disorders are eligible for this study. Representative types of patients include those with: - Plasma cholesterol levels greater than 200 mg/dl or less than 120 mg/dl - Plasma LDL-C levels greater than 130 mg/dl or less than 70 mg/dl - Plasma HDL-C levels greater than 70 mg/dl or less than 25 mg/dl - Unusual cholesterol deposits or xanthomas (nodules of lipid deposits on the skin) Children under 2 years of age are excluded from the study. Participants will undergo some or all of the following procedures: - Plasma evaluation. Apolipoproteins (plasma proteins involved in metabolism of cholesterol, triglycerides, phospholipids, and proteins in the blood) and enzymes involved in lipid metabolism are measured. - Fat biopsy. A small sample of fat tissue is collected for examination. For this test, an area on the buttock or abdominal wall is numbed. A needle is inserted into the fat, and a small amount of tissue is sucked out by a syringe. - Leukapheresis. White blood cells are collected to help diagnose the lipid disorder. For this test, blood is collected through a needle in an arm vein, similar to donating blood. The blood circulates through a machine that separates it into its components, and the white cells are removed. The rest of the blood is returned to the body, either through the same needle or through another needle in the other arm. - Skin biopsy. Skin cells are collected for study. The cells are grown in the laboratory and the amount of cholesterol that enters or leaves the cells is measured, providing information on abnormalities in cholesterol transport. For this test, an area of skin is numbed with an anesthetic and a small circular area is removed, using a skin punch instrument similar to a sharp cookie cutter. - Heparin infusion study. Heparin, a blood thinner, releases enzymes that break down fat in the blood. Lipase activity (breakdown of fats) in the blood is measured following the injection of heparin into a vein.

NCT ID: NCT00349765 Completed - Clinical trials for Hypercholesterolemia

Effects of Various Higher Fat and Lower Fat Snacks on Cardiovascular Risk Factors in Men and Women.

Start date: March 2005
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether snacks differing in fat amount and type result in changes in cardiovascular disease risk factors in men and women who have mildly elevated cholesterol levels. Our hypothesis is that a diet containing snacks rich in polyunsaturated fats lead to a more favorable cardiovascular disease risk profile than a diet containing snacks rich in saturated and trans fats or one containing low-fat snacks.

NCT ID: NCT00347217 Completed - Hypercholesteremia Clinical Trials

Observational to Investigate the Efficacy of CRESTOR 5mg in Reaching LDL-C Target Goals in Patients Who Are at High Risk for a Cardiovascular Event

Start date: February 2006
Phase: Phase 4
Study type: Observational

Observational study to investigate the use and efficacy of CRESTOR 5 mg in reaching LDL-C target goals in both statin naïve and statin treated primary and secondary prevention patients at high risk for a cardiovascular event.

NCT ID: NCT00345722 Completed - Clinical trials for Cardiovascular Diseases

The Effect of Strawberries in a Cholesterol-Lowering Dietary Portfolio

Start date: June 2006
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether addition of strawberries to a dietary portfolio of cholesterol-lowering foods will improve compliance and so increase the effectiveness of the dietary portfolio in lowering cholesterol and improving cardiovascular risk factors.

NCT ID: NCT00344175 Completed - Clinical trials for Hypercholesterolemia

Follow-on Protocol of Pitavastatin Versus Simvastatin in Patients With Hypercholesterolemia or Dyslipidemia and Coronary Heart Disease Risk Factors

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

This is a sixteen-week follow-on and 28 week single-blind extension study for patients who participated in study NK-104-304.