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Dyslipidemias clinical trials

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NCT ID: NCT00325780 Completed - Clinical trials for Hypercholesterolemia

Long-Term Extension Study of Pitavastatin in Patients With Primary Hypercholesterolemia or Combined Dyslipidemia

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

This study is a long-term follow-up protocol for patients who participated in study NK-104-3.01EU or study NK-104-3.02EU.

NCT ID: NCT00316095 Completed - Hypertension Clinical Trials

Combination of Telmisartan and Simvastatin in the Treatment of Hypertension and Hypercholesterolemia

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

This study will investigate two registered drugs, one for the treatment of high blood pressure and one for the treatment of elevated cholesterol. High blood pressure (hypertension) is a common medical condition affecting millions of people worldwide. A wide variety of effective drug treatments is available to reduce blood pressure. Elevated cholesterol (hypercholesterolemia) is a common medical condition affecting people worldwide. A wide variety of effective drug treatments is available to reduce cholesterol levels. Hypertension and hypercholesterolemia often occur together. They are both important risk factors for the development of heart and vessel diseases (e.g. heart attack or stroke). Current guidelines advise treatment of high blood pressure and elevated cholesterol to reduce the risk of cardiovascular diseases. This study will test the simultaneous use of a drug to reduce blood pressure and a drug to reduce elevated cholesterol. Both drugs are registered and are effective. The drug for treatment of high blood pressure is telmisartan Micardis). The drug for treatment of elevated cholesterol is simvastatin (Zocor). Since hypertension and hypercholesterolemia frequently occur together, the purpose of this study is to investigate whether both drugs can be used simultaneously. A low dose and a high dose of these drugs will be used. It will be investigated whether each of the drugs is still as effective when given together, at the same time of day, with the other drug.

NCT ID: NCT00312923 Completed - HIV Infections Clinical Trials

Preliminary Study of Safety and Efficacy of Policosanol

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

Lay Language Summary: High cholesterol levels are common in persons with HIV infection. However, conventional cholesterol-lowering medications may have harmful side effects when given to HIV-infected persons. Therefore, we plan to evaluate the safety and effectiveness of policosanol, a dietary supplement derived from sugar cane that has cholesterol-lowering properties, to lower cholesterol levels in persons with HIV infection. We hypothesize that policosanol will lower levels of LDL cholesterol ("bad" cholesterol) and raise levels of HDL cholesterol ("good" cholesterol).

NCT ID: NCT00309777 Completed - Clinical trials for Hypercholesterolemia

Study to Compare the Efficacy and Safety of Pitavastatin and Simvastatin

Start date: September 2005
Phase: Phase 3
Study type: Interventional

The purpose of this study is to compare the efficacy and safety of pitavastatin with that of simvastatin.

NCT ID: NCT00309751 Completed - Dyslipidemia Clinical Trials

Study Comparing Pitavastatin and Atorvastatin in Patients With Type II Diabetes Mellitus and Combined Dyslipidemia

Start date: December 2005
Phase: Phase 3
Study type: Interventional

The purpose of this study is to compare the efficacy and safety of pitavastatin with that of atorvastatin in patients with type II diabetes mellitus (type II DM) and combined dyslipidemia.

NCT ID: NCT00309738 Completed - Clinical trials for Hypercholesterolemia

Study to Compare the Efficacy and Safety of Pitavastatin and Simvastatin

Start date: September 2005
Phase: Phase 3
Study type: Interventional

The purpose of this study is to compare the efficacy and safety of pitavastatin with that of simvastatin in patients with risk factors for heart disease.

NCT ID: NCT00309712 Completed - Clinical trials for Type II Diabetes Mellitus

Diabetes and Combined Lipid Therapy Regimen (DIACOR) Study

Start date: August 2002
Phase: N/A
Study type: Interventional

The primary study hypothesis of this study is to determine whether there is a greater percentage of patients achieving a triglyceride level of <200 mg/dL with the combination of simvastatin 20 mg and fenofibrate 160mg than with either simvastatin 20 mg monotherapy or fenofibrate 160mg monotherapy.

NCT ID: NCT00304993 Completed - Insulin Resistance Clinical Trials

Study of Niacin and Rosiglitazone in Dysmetabolic Dyslipidemia

Start date: January 2001
Phase: Phase 4
Study type: Interventional

Lipid abnormalities in people with the Metabolic Syndrome (the Insulin Resistance Syndrome) are characterized by elevations in triglycerides and LDL cholesterol; low levels of HDL cholesterol; and small, dense LDL particles. Statins generally do not change LDL particle size, so often fenofibrate is added. This combination may still not be sufficient. Niacin is a common third drug added to the treatment regimen, but niacin can increase insulin resistance. This study compares niacin as a third drug to rosiglitazone, an insulin sensitizer.

NCT ID: NCT00300482 Completed - Clinical trials for Coronary Heart Disease

Evaluate Safety and Efficacy of ABT-335 in Combination With Rosuvastatin Calcium in Subjects With Multiple Abnormal Lipid Levels in the Blood

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

The purpose of this study is to compare the safety and efficacy of fenofibric acid (ABT-335) + rosuvastatin calcium combination therapy with ABT-335 and rosuvastatin calcium monotherapy in subjects with multiple abnormal lipid levels in the blood.

NCT ID: NCT00300469 Completed - Clinical trials for Coronary Heart Disease

Evaluate Safety and Efficacy of ABT-335 in Combination With Atorvastatin in Subjects With Multiple Abnormal Lipid Levels in the Blood

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

The purpose of this study is to compare the safety and efficacy of fenofibric acid (ABT-335) + atorvastatin combination therapy with ABT-335 and atorvastatin monotherapy in subjects with multiple abnormal lipid levels in the blood.