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Hyperlipoproteinemias clinical trials

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NCT ID: NCT01811082 Completed - Clinical trials for Hyperlipoproteinemia

Comparison of Coenzyme A and Pantethine Capsule for Safety and Efficacy On Patients With Hyperlipidemia

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

The purpose of this study is to compare the lipid lowering effects and clinical safety of a natural hypolipidemic compound, coenzyme A capsule with a marketed drug, Pantethine Capsule, in Chinese patients with moderate dyslipidemia.

NCT ID: NCT01763918 Completed - Hyperlipidemia Clinical Trials

Reduction of LDL-C With PCSK9 Inhibition in Heterozygous Familial Hypercholesterolemia Disorder Study-2

RUTHERFORD-2
Start date: February 7, 2013
Phase: Phase 3
Study type: Interventional

The primary objective was to evaluate the effect of 12 weeks of evolocumab subcutaneously once every 2 weeks (Q2W) and once monthly (QM), compared with placebo, on percent change from baseline in low-density lipoprotein cholesterol (LDL-C) in adults with heterozygous familial hypercholesterolemia (HeFH).

NCT ID: NCT01753232 Completed - Clinical trials for Hypercholesterolemia, Familial

Safety and Efficacy of the DALI LDL-adsorber and MONET Lipoprotein Filter

LINET
Start date: May 2012
Phase: N/A
Study type: Observational

Low Density Lipoprotein (LDL)-apheresis refers to a procedure in which blood taken from a patient's vein is cleaned from pathogenic substances, e.g. cholesterol, outside the body and then given back to the patient. In the DALI (Direct Adsorption of Lipoproteins)-system whole blood is pumped over an adsorber containing beads that selectively bind LDL-cholesterol. The MONET (Membrane filtration Optimized Novel Extracorporeal Treatment)-system works with plasma which is cleaned by filtration. This study comprises the recording of safety and efficacy data from patients treated either with the DALI or MONET-system over a period of 2 years.

NCT ID: NCT01695954 Completed - HIV Clinical Trials

Pharmacokinetic Study of Pitavastatin and Ritonavir-Boosted Darunavir or Efavirenz

Start date: May 2012
Phase: Phase 1
Study type: Interventional

The main goal of this study is to determine how taking efavirenz affects the levels of pitavastatin in the bloodstream when both drugs are taken together and to see how darunavir with ritonavir affects the levels of pitavastatin in the bloodstream. Secondary goals are to see how taking pitavastatin affects the levels in the blood of efavirenz when both drugs are taken together and to see how taking pitavastatin affects the levels in the blood of darunavir.

NCT ID: NCT01671254 Completed - Hyperlipidemia Clinical Trials

Effect of Citrus Bioflavonoids/Vitamin E in Conjunction With Fish Oil Supplementation

Start date: August 2012
Phase: N/A
Study type: Interventional

The purpose of this 8-week intervention trial is to investigate the effect of a dietary supplement (containing citrus bioflavonoids and vitamin E) plus fish oil supplementation in healthy hyperlipidemic subjects

NCT ID: NCT01645046 Completed - Clinical trials for Hyperlipoproteinemia

The Effects of Coenzyme A on Serum Lipids in Patients With Hyperlipidemia

Start date: October 2008
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the lipid lowering effects and clinical safety of a natural hypolipidemic compound, coenzyme A (CoA) capsule in Chinese patients with moderate dyslipidemia.

NCT ID: NCT01607294 Completed - Type 2 Diabetes Clinical Trials

A Single Center Study to Evaluate the Efficacy and Safety of ETC 1002 in Subjects With Type 2 Diabetes

Start date: April 2012
Phase: Phase 2
Study type: Interventional

This Phase 2 study will asses the LDL-C lowering efficacy of ETC-1002 versus placebo in subjects with type 2 diabetes.

NCT ID: NCT01606930 Completed - Hypertension Clinical Trials

A Pilot Study to Improve Patient-Doctor Communication

Start date: November 2010
Phase: N/A
Study type: Interventional

The purpose of this controlled pilot study is to determine whether an intervention aimed at patients will improve partnering, shared decision-making and open communication. Results from this pilot study will inform how to best proceed with a larger multi-centered randomized controlled trial. The specific hypothesis for this pilot study is to: 1. Test the feasibility of a simple patient-centered intervention. 2. Test the correlation between patient readiness to actively engage in conversation (assessed using a pre-visit patient survey) and actual patient behaviors in the encounter. 3. Develop a coding tool that will quantify patient activation in clinical encounters. 4. Test whether activating patients who are more involved and revealing in the patient-clinician dyad will improve patient and clinician outcomes.

NCT ID: NCT01592084 Completed - Clinical trials for Amyotrophic Lateral Sclerosis

Hyperlipidemia and Statin Therapy in Amyotrophic Lateral Sclerosis

Start date: April 2008
Phase: N/A
Study type: Observational

The role of hyperlipidemia and lipid lowering therapy (LLT) in Amyotrophic Lateral Sclerosis (ALS) pathophysiology and its impact on disease progression and survival is unclear. The investigators analyzed the correlation between lipid levels with disease progression and survival in ALS patients and the association of LLT with these outcomes.

NCT ID: NCT01524289 Completed - Clinical trials for Hypercholesterolemia, Familial

Study to Assess the Tolerability and Efficacy of Anacetrapib (MK-0859) Co-Administered With Statin in Participants With Heterozygous Familial Hypercholesterolemia (MK-0859-020)

REALIZE
Start date: February 3, 2012
Phase: Phase 3
Study type: Interventional

The objective of this study is to evaluate the efficacy and tolerability of adding anacetrapib to ongoing statin therapy in participants with heterozygous familial hypercholesterolemia (HeFH).