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Hypercholesterolemia clinical trials

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NCT ID: NCT01779687 Completed - HIV Clinical Trials

Pharmacokinetic Drug Interaction Study Between Raltegravir and Atorvastatin.

AVIATOR
Start date: March 2013
Phase: Phase 1
Study type: Interventional

Dyslipidemia is highly prevalent among patients with HIV infection and contributes to the increased cardiovascular disease risk in this patient population. Atorvastatin lowers plasma low-density lipoprotein (LDL) cholesterol levels and is used for prevention of artherosclerotic disease. Raltegravir, an HIV integrase inhibitor, could be one of the preferred antiretroviral agents in HIV patients with dyslipidemia because it has a beneficial lipid profile. Theoretically, no clinically relevant drug interaction is expected between atorvastatin and raltegravir. However, atorvastatin and raltegravir share similar metabolic pathways which could be relevant in the occurrence of pharmacokinetic interactions. In order to be able to recommend raltegravir and atorvastatin concomitant use, a pharmacokinetic study in healthy volunteers is proposed.

NCT ID: NCT01779453 Completed - Clinical trials for Hypercholesterolemia

A Study of the Safety, Pharmacokinetic Drug Interaction and Efficacy of ETC-1002 and Atorvastatin in Subjects With Hypercholesterolemia

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

This study will assess the safety, atorvastatin pharmacokinetics, and LDL-C lowering efficacy of ETC-1002 versus placebo in hypercholesterolemic subjects on background therapy of atorvastatin 10 mg.

NCT ID: NCT01768403 Completed - Hypertension Clinical Trials

Centralised Pan-Algerian Survey on the Undertreatment of Hypercholesterolemia

CEPHEUS
Start date: September 2010
Phase: N/A
Study type: Observational

Centralized Pan-Algerian Survey on the undertreatment of hypercholesterolemia. The purpose of this study is to establish the proportion of patients on lipid-lowering pharmacological treatment reaching the LDL-C goals according to the Third Joint European Task Force guidelines in the survey population.

NCT ID: NCT01767077 Completed - Clinical trials for Hypercholesterolemia

Role of Milk Fat Globule Membranes in Dairy Foods: Health Effects in Humans

MFGM
Start date: February 2013
Phase: N/A
Study type: Interventional

Investigate the effects of milk fat with or without milk fat globule membranes (MFGM) on blood lipid profile, vascular function, insulin sensitivity, inflammation and gene expression. Overweight subjects will be randomized to one of 2 groups with different types of dairy products: 1)butter oil; 2) cream (milk fat with MFGM).

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: NCT01751984 Completed - Clinical trials for Hypercholesterolemia

A Study of the Efficacy and Safety of ETC-1002 in Participants With Statin Intolerance

Start date: October 4, 2012
Phase: Phase 2
Study type: Interventional

This study will assess the Low-Density Lipoprotein-Cholesterol (LDL-C) lowering efficacy and safety of ETC-1002 versus placebo in participants with hypercholesterolemia and a history of statin intolerance.

NCT ID: NCT01744977 Completed - Clinical trials for Hypercholesterolemia

Cholesterol Medication Packaging Study

MWV_CAPS
Start date: December 2012
Phase: N/A
Study type: Interventional

The purpose of the overall study is to improve medication use rates among veterans by looking at the risk factors of low-density lipoprotein cholesterol (LDL). It will involve patients who have high LDL-C level (<130mg/dl) and /or may have difficulty taking their medications based on how often they refilled their medications in the last 12 months. The investigators will test an innovative adherence packaging relative to usual care. The primary hypothesis is that veterans who receive the intervention will have greater improvement in their medication adherence as measured by pill refill at 6 and 12 months of follow up as compared to the control group.

NCT ID: NCT01744392 Completed - Hypertension Clinical Trials

Medication Adherence With Polyglot Meducation

Start date: February 2013
Phase: N/A
Study type: Interventional

The investigators propose a 6 month pre-post, pilot,feasibility study with up to 25 individuals among veterans with cardiovascular disease risk factors including Hypertension (HT), Diabetes Mellitis (DM) and Hyperlipidemia (HL) who receive care from the hospital-based primary care clinics associated with Durham VAMC. The investigators will examine veteran's perception and ease of using an innovative tool to help improve medication adherence to cardiovascular medications. This study aims to focus on patients with multiple chronic conditions and their caregivers to address 1) appropriate use of medications 2)maximize patient self-care and care by families and other caregivers 3) make available a tool for medication management 4) managing complex regimens, and 5) addressing health literacy.

NCT ID: NCT01743313 Terminated - Clinical trials for Hypercholesterolemia

Glucose Metabolism Disorders and Metabolic Syndrome Before and After Primary Hip and Knee Replacement

HyTe-2
Start date: April 2012
Phase:
Study type: Observational

Osteoarthritis patients undergoing primary hip and knee replacement are followed-up and changes in their glucose metabolism and other metabolic parameters (obesity, cholesterol levels) are examined. Persistent postoperative pain is examined as secondary outcome.