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Hyperlipoproteinemia Type II clinical trials

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NCT ID: NCT01078675 Completed - Clinical trials for Familial Hypercholesterolaemia

An Study to Evaluate Rosuvastatin in Children and Adolescents With Familial Hypercholesterolaemia

Start date: February 2010
Phase: Phase 3
Study type: Interventional

This study is being carried out to see if the study medication, rosuvastatin, is effective in treating familial hypercholesterolaemia in children and adolescents, and to determine the long term (over 2 years) safety, tolerability and efficacy of the study medication in these patients. This study will also measure levels of drug in the blood and see how well it is tolerated. This is known as pharmacokinetic (PK) analysis. At baseline only a small number of patients will participate in a single dose PK phase over 24 hours. In order to see if this medication works, a control group of healthy siblings will help the researchers to compare certain results.

NCT ID: NCT01070966 Completed - Clinical trials for Primary Hypercholesterolemia and Homozygous Familial Hypercholesterolemia (HoFH)

Vytorin Reexamination Study (0653A-174)

Start date: July 2005
Phase:
Study type: Observational

This survey is conducted for preparing application material for re-examination under the Pharmaceutical Affairs Laws and its Enforcement Regulation, its aim is to reconfirm the clinical usefulness of VYTORIN through collecting the safety and efficacy information according to the Re-examination Regulation for New Drugs.

NCT ID: NCT00943306 Completed - Clinical trials for Familial Hypercholesterolemia

Long Term, Follow-on Study of Lomitapide in Patients With Homozygous Familial Hypercholesterolemia

Start date: October 29, 2009
Phase: Phase 3
Study type: Interventional

This was a long term follow on study to assess the continued long term safety and efficacy of lomitapide in patients with homozygous familial hypercholesterolemia.

NCT ID: NCT00924339 Not yet recruiting - Clinical trials for Familial Hypercholesterolemia

Soy Food Intervention Trial

SOYFIT
Start date: September 2009
Phase: N/A
Study type: Interventional

Familial hypercholesterolemia (FH MIM#143890), an inherited disorder of lipoprotein metabolism, is a risk for early cardiovascular disease (CVD). This autosomal dominant disease is characterized by markedly elevated plasma concentrations of low density lipoprotein (LDL) and total cholesterol (TC), typically well above the 95th percentile for age and sex (1). A defective gene for the LDL-receptor is inherited from one parent (2). The disorder was first noted by Müller in 1939, including familial clustering of tendon xanthomas, high serum cholesterol and early MIs (3). The present study aims: a) to strengthen the evidence for the hypocholesterolaemic effect of soy protein in children and adolescents affected with FH b) to monitor the compliance of soy consumption as a possible causal factor linked to the variable lipaemic response observed in the previous study c) to assess certain safety markers of soy food consumption (hormone status, thyroid function, bone metabolism) 4) to monitor the adherence to the soy intervention additionally comprise collections of blood and urine samples. Hypothesis 1: Soya protein-substituted diets change total and LDL-cholesterol, Apolipoprotein B and uric acid serum concentrations. Primary parameters: Blood analysis Hypothesis 2: Children and adolescents with FH, in which the cholesterol, LDL-lipoprotein and Apolipoprotein B concentration is not influenced by means of soy protein substituted diet - is it because of a) the effect of non-responder? or b) subjects, who have no regularly dietary soya intake. Secondary parameters: isoflavones daidzein, glycetein, genistein and equol in the urine samples

NCT ID: NCT00924274 Recruiting - Clinical trials for Familial Hypercholesterolemia

Effect of Rapeseed Oil and Sunflower Oil

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

Familial hypercholesterolemia (FH), an inherited disorder of lipoprotein metabolism, is a risk for early cardiovascular disease (CVD). This autosomal dominant disease is characterized by markedly elevated plasma concentrations of low density lipoprotein (LDL) and total cholesterol (TC). The purpose of this study is to compare the effect of a diet low in saturated fats but enriched either with rapeseed oil (RO) or sunflower oil (SO) in children and adolescents with FH on serum lipoproteins.

NCT ID: NCT00916643 Completed - Clinical trials for Familial Hypercholesterolemia

Low-Density Lipoprotein (LDL) Apheresis Using H.E.L.P. Therapy

Secura
Start date: December 1999
Phase: Phase 4
Study type: Interventional

The objectives of this post-surveillance study are to continue to evaluate the safety and effectiveness of the H.E.L.P. System. The safety and effectiveness will be assessed by evaluating the occurrence of death, cardiovascular events or interventions, angina, and serious unanticipated adverse effects. Laboratory assessments will be made to document low-density lipoprotein cholesterol (LDL-C) reduction and any effects on other blood components. Quality of life assessments will also be made. The study will also assess the modifications to the H.E.L.P. System, including: - use of a single heparin adsorber, instead of two smaller adsorbers; - change in the supplier of the ultrafilter (from Secon to Toray); - reduction in the number of blood lines from eleven to nine; - change from a single-layer to a two-layer precipitate filter. The safety and efficacy of the device specific to these modifications will be evaluated by comparing the safety and efficacy data from the patient registry to the data from the initial clinical study on the device as originally designed.

NCT ID: NCT00827606 Completed - Clinical trials for Familial Hypercholesterolemia

Atorvastatin Three Year Pediatric Study

Start date: March 2009
Phase: Phase 3
Study type: Interventional

The purpose of this study is to characterize three year descriptive growth and development (ie, height, weight, body mass index, Tanner Stage) and efficacy of cholesterol reduction in pediatric subjects with Heterozygous Familial Hypercholesterolemia receiving atorvastatin treatment.

NCT ID: NCT00751608 Withdrawn - Clinical trials for Familial Hypercholesterolemia

Effect of APL180 on Endothelial Function in Familial Hypercholesterolemia Patients

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

This study will evaluate the effect of APL180 on endothelial function measured by forearm venous occlusion plethysmography in patients with familial hypercholesterolemia.

NCT ID: NCT00739999 Completed - Clinical trials for Pediatric Heterozygous Hypercholesterolemia

8-Week PK/PD Atorvastatin Study In Children And Adolescents With Heterozygous Familial Hypercholesterolemia

Start date: December 2008
Phase: Phase 1
Study type: Interventional

To evaluate pharmacokinetics, pharmacodynamics, safety and tolerability of atorvastatin in children and adolescents with heterozygous familial hypercholesterolemia

NCT ID: NCT00730236 Completed - Clinical trials for Homozygous Familial Hypercholesterolemia

A Safety and Efficacy Study of AEGR-733 to Treat Homozygous Familial Hypercholesterolemia (FH)

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

The goal of this trial is to study the effects of AEGR-733 on LDL cholesterol, other lipids as well as measures of safety over the long-term.