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Hypercholesterolemia clinical trials

View clinical trials related to Hypercholesterolemia.

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NCT ID: NCT00529178 Completed - Clinical trials for Hypercholesterolemia

Pravastatin Efficacy and Safety Trial in Hypercholesterolemic Patients With Chronic Liver Disease

Start date: December 2002
Phase: Phase 4
Study type: Interventional

To determine in hypercholesterolemic subjects with chronic, well-compensated liver disease, the percent change from baseline to Week 12 in serum LDL-C of pravastatin 80 mg compared to placebo.

NCT ID: NCT00526721 Completed - Clinical trials for Hypercholesterolemia

Real-life EValuation Of High Dose RosUvastatin in High Risk Patients After TitraTION

REVORUTION
Start date: May 2007
Phase: N/A
Study type: Observational

To evaluate achievement ratio of treatment target goal in hypercholesterolemia patients with high risk after high dose rosuvastatin(20mg/day) titration

NCT ID: NCT00526058 Completed - Clinical trials for Hypercholesterolemia

(H.E.L.P.)Apheresis Therapy to Compare the Reduction of LDL (Low Density Lipoprotein) Cholesterol

FUTURA
Start date: August 2007
Phase: N/A
Study type: Interventional

The primary objective of the study is to demonstrate that the performance of the modified Plasmat® Futura H.E.L.P. Apheresis System is non-inferior to the current FDA approved Plasmat® Secura H.E.L.P Apheresis System for use under the approved indication of the acute reduction of LDL-cholesterol from the plasma in populations for whom diet has been ineffective and maximum drug therapy has either been ineffective or not tolerated.

NCT ID: NCT00525824 Completed - Atherosclerosis Clinical Trials

12-week Open-label, Phase IIIb Comparing Efficacy and Safety of Rosuvastatin (CRESTORâ„¢) in Combination With Ezetimibe

GRAVITY
Start date: August 2007
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine whether treatment of Rosuvastatin (CRESTORâ„¢) or Simvastatin given as monotherapy or given in combination with Ezetimibe, will lower the Low Density Lipoprotein Cholesterol (LDL-C) in patients with Hypercholesterolaemia and Coronary Heart Disease (CHD) or a CHD Risk Equivalent, Atherosclerosis or a 10-year CHD Risk of >20%

NCT ID: NCT00523796 Completed - Clinical trials for Hypercholesterolemia

InPractice Survey on the Treatment of Hypercholesterolemia

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

This is a multi-centre survey of patients who are currently on lipid-lowering pharmacological treatment. Data collection for each patient will take place at one visit.

NCT ID: NCT00515307 Completed - Clinical trials for Hypercholesterolemia, Familial

Bone Marrow Stem Cells as a Source of Allogenic Hepatocyte Transplantation in Homozygous Familial Hypercholesterolemia

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

Patients with homozygous familial hypercholesterolemia has very high serum cholesterol levels despite receiving lipid lowering drugs (e.g. statins, etc). Most of such patients die before the age of 20 due to myocardial infarction, etc. Orthotopic liver transplantation (OLT) is an effective treatment for that. Hepatocyte transplantation is an alternative to OLT that may help to overcome the shortage of donor organs. There have been reports of successful treatment of different kinds of metabolic liver disorders by hepatocyte transplantation. The major problem with hepatocyte transplantation is that the source of hepatocytes is very limited. Bone marrow stem cells are the potential source of hepatocytes. In the in-vitro culture system successful and efficient transdifferentiation of mesenchymal stem cells into hepatocytes has been documented. We have already shown that infusion of mesenchymal stem cells is safe and feasible in cirrhosis (Mohamadnejad M, et al. Arch Iran Med 2007; In Press). In this study, 2 patients with homozygous familial hypercholesterolemia will be included. The bone marrow of healthy volunteers with a normal lipid profile will be taken, then bone marrow mesenchymal stem cells (MSCs) will be cultured, and then MSCs will be trans-differentiate into hepatocytes, and the cells will be infused through the portal vein into the patients. The duration of follow up will be 6 months post-transplantation.

NCT ID: NCT00510809 Completed - High Cholesterol Clinical Trials

Effect of Policosanol as Monotherapy and Adjunctive to Statin Therapy

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

To determine the effects of policosanol on the cholesterol profile.

NCT ID: NCT00502047 Completed - Clinical trials for Cardiovascular Disease

Effect of the Plantago Ovata Husk on the Lipid Profile of Patients With Hypercholesterolemia

Start date: September 2005
Phase: Phase 2/Phase 3
Study type: Interventional

The hypothesis of this study is that soluble fibre may contribute to a reduction of the low density lipoprotein cholesterol (LDL-c), and the combined effect with a statin may achieve an optimisation of the cholesterol-lowering effects in adults with several cardiovascular risk factors.

NCT ID: NCT00496730 Completed - Clinical trials for Hypercholesterolemia

A Multicenter, Randomized, Open Label Study to Evaluate the Lipid Lowering Efficacy and Safety of Vytorin® 10/20 vs. Atorvastatin 10mg in Hypercholesterolemia Patients With Metabolic Syndrome in Korea (0653A-129)(COMPLETED)

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

Prevalence of metabolic syndrome in korea is increasing. There is no clinical trial targeting on such increasing populations like metabolic syndrome patients with Vytorin® in korea. Therefore this trial will help evaluate the lipid lowering effect of Vytorin® in asian population with metabolic syndrome.

NCT ID: NCT00493337 Completed - Clinical trials for Hypercholesterolemia

A Community Pharmacist-led Intervention to Improve Adherence to Lipid-lowering Treatment

Start date: May 2008
Phase: N/A
Study type: Interventional

The objective of the study is to test the effectiveness of a community pharmacist-led intervention to increase adherence to lipid lowering treatment.