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Hyperlipidemias clinical trials

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NCT ID: NCT00781560 Completed - Hyperlipidemia Clinical Trials

Awareness of Chinese National Adult Lipid Treatment Guideline (2007) and Rate of Patients Achieving the Treatment Goal

CRE NIS
Start date: October 2008
Phase: N/A
Study type: Observational

This study is designed to survey the awareness rate of Chinese National Adult Lipid Treatment Guideline (2007) by cardiologists; To survey the control rate of the patients with dyslipidemia in "real world"; and to evaluate the percentage of hyperlipidemia patients who achieved target LDL-C level according to the Chinese National Adult Lipid Treatment Guideline (2007) following 8-week treatment by Crestor® 5mg or 10mg

NCT ID: NCT00778804 Completed - Hypertension Clinical Trials

Preventing Heart Disease in Underserved Patients

Start date: July 2004
Phase: N/A
Study type: Interventional

The study will evaluate the impact of an internet based telemedicine system on cardiovascular risk profile of underserved patient populations. It is our hypothesis that a treatment plan and frequent communication via an internet based Telemedicine system will improve the cardiovascular risk profile of underserved patient populations at increased risk for cardiovascular disease. Our primary endpoint is a reduction over one year in the 10-year CVD risk score (ATP III risk model).

NCT ID: NCT00758303 Completed - Hyperlipidemia Clinical Trials

A Study to Evaluate the Lipid Regulating Effects of TRIA-662

Start date: September 2007
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to determine the effectiveness and safety of TRIA-662 (also known as 1-MNA) in treating elevated triglyceride levels in patients not receiving lipid lowering treatment. This study will determine the effects of TRIA-662 on commonly measured blood fats that are known to be important in the prevention of vascular disease.

NCT ID: NCT00756405 Completed - Obesity Clinical Trials

Effects of Dietary Antioxidants on Cardiovascular Risk Factors

Start date: March 2007
Phase: N/A
Study type: Interventional

The aim of the Antioxidant Study was to compare the efficacy of foods naturally rich in antioxidants with that of antioxidants in a pill form on markers of inflammation and plasma cholesterol in healthy adults at risk of cardiovascular disease.

NCT ID: NCT00754039 Completed - Clinical trials for Hypercholesterolemia

Study to Compare Welchol and TriCor to TriCor Alone in Patients With High Cholesterol

Start date: February 2003
Phase: Phase 4
Study type: Interventional

The primary objective of this study is to compare the effect of Welchol in combination with TriCor compared to TriCor alone on low-density lipoprotein cholesterol (LDL-C) in patients with high cholesterol.

NCT ID: NCT00753883 Completed - Hyperlipidemia Clinical Trials

Ezetrol Post-Marketing Study

Start date: July 2006
Phase: Phase 4
Study type: Interventional

To compare the lipid lowering efficacy of adding ezetimibe to statin vs. statin alone.

NCT ID: NCT00749801 Completed - Hyperlipidemia Clinical Trials

Efficacy and Safety of Geneferm Nattokinase

Start date: May 2007
Phase: N/A
Study type: Interventional

Nattokinase, first found by Dr. Hiroyuki Sumi in 1980, is a potent fibrinolytic enzyme extracted from Natto, a popular soybean fermented food in Japan. It was confirmed that oral administration of nattokinase (or natto) produced a mild and frequent enhancement of the fibrinolytic activity in the plasma as indicated by the fibrinolytic parameters and the production of tissue plasminogen activator. Other studies also showed a reduction in lipid peroxidation and improvement of lipid metabolism. Short-term effect (less then 10 days) of oral administration of nattokinase on both animal and human subjects has been studied and reported. However, whether nattokinase possesses a beneficial effect to dyslipidemic patients remains unclear. The aim of this study is to investigate the long-term effect (six month) of the mono and multiple formulae of nattokinase, change of BP, lipid and fibrinolytic factors from baseline and 6 months on dyslipidemic patients.

NCT ID: NCT00726362 Completed - Hyperlipidemias Clinical Trials

To Explore the Treatment Effect of Various Commercially Available Statins on Patients With Hyperlipidemia

Start date: December 2007
Phase: N/A
Study type: Observational

The primary objective is to survey the efficacy of various commercially available statins (a class of lipid-lowering agents, for example, rosuvastatin, atorvastatin, simvastatin, lovastatin, pravastatin and fluvastatin) under local clinical practice in treating patients with hyperlipidemia. Surveillance data (Lipid Profile) will be collected during course of usual clinical practice or captured upon its availability.

NCT ID: NCT00723723 Completed - Clinical trials for Hypercholesterolemia

Compliance With LDL-Lowering Therapy (Study P05467)(COMPLETED)

Start date: January 2008
Phase:
Study type: Observational

This observational study is being conducted in patients receiving statin treatment as secondary prevention of coronary heart disease under the current standard of care in compliance with European guidelines. The purpose of the study is to evaluate the percentage of these patients that reach target LDL levels. Additionally this study will measure the patient's compliance to treatment as assessed by counting the returned tablets. Both assessments will be made at visits conducted 6-8 weeks after the first visit and 28-32 weeks after the first visit.

NCT ID: NCT00713167 Completed - Hyperlipidemia Clinical Trials

The Efficacy of Red Grape Seed Extract on Lipid Profile and Oxidized Low-Density Lipoprotein (OX-LDL)

GSE
Start date: July 2008
Phase: Phase 2/Phase 3
Study type: Interventional

Antioxidants are potent scavengers of free radicals and serve as inhibitors of neoplastic processes. A large number of synthetic and natural antioxidants are known to induce beneficial effects on human health and disease prevention. Cardioprotective ability of grape seed extract polyphenols (GSEP) was studied in animals and humans. It has been suggested that grape seed proanthocyanidins have cardioprotective effects against reperfusion-induced injury of free radicals after ischemia. In another study, it is suggested that proanthocyanidins, the major polyphenols in red wine, might trap reactive oxygen species in aqueous series such as plasma and interstitial fluid of the arterial wall; thereby inhibiting oxidation of low-density lipoprotein (LDL) and showing an antiatherosclerotic activity. The only human model study designed to evaluate the effect of a standardized formulation of a GSEP (leucoselect-phytosome [LP]) on the susceptibility of LDL to oxidation in a group of heavy smokers, revealed that the antioxidant potential of GSEP may be effective in oxidative stress (smoking); however more investigational data are needed before wider use in clinical settings. Based on these observations, the investigators decided to evaluate the effect of GSEP in reducing OX-LDL in patients diagnosed with mild hyperlipidemia.