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Hyperlipidemias clinical trials

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NCT ID: NCT00955227 Active, not recruiting - Clinical trials for Hypercholesterolemia

Can Cholesterol Lowering Drugs Influence Circulating Omega-3 Fatty Acid Levels

Start date: July 2009
Phase: N/A
Study type: Interventional

The objective of this study is to determine if the administration of a cholesterol lowering drug like ezetimibe will reduce circulating omega-3 fatty acid (ALA) levels in patients with heart disease and hypercholesterolemia. The investigators hypothesize that their data will discover that patients receiving ezetimibe require additional dietary supplementation with omega-3 supplements to insure that these beneficial fatty acids are available to these patients.

NCT ID: NCT00947635 Completed - Clinical trials for Diabetes Mellitus, Type 1

Cholesterol and Fatty Acid Synthesis in Islet and Liver Transplant Patients and Effect of Dietary Intervention

Start date: November 2005
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose is to investigate possible mechanisms of increased blood lipid levels following transplantation, and also to see if a comprehensive dietary intervention is effective in reducing blood lipid levels in post-transplant patients.

NCT ID: NCT00941603 Completed - Clinical trials for Primary Hypercholesterolemia

Phase 2 Dose-Ranging Efficacy and Safety Trial of SCH 900271 in Participants With Primary Hypercholesterolemia or Mixed Hyperlipidemia (P05675)

Start date: June 29, 2009
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the effect of SCH 900271 compared to placebo on the reduction of low-density lipoprotein cholesterol (LDL-C) from baseline to 8 weeks of treatment in participants with primary hypercholesterolemia (familial and nonfamilial) or mixed hyperlipidemia. The study will also evaluate the effect of SCH 900271 on non-high density lipoprotein cholesterol (non-HDL-C) and various other lipids and lipoproteins. The safety of SCH 900271 in this participant population will also be evaluated.

NCT ID: NCT00938405 Completed - Clinical trials for Diabetes Mellitus, Type 1

Efficacy of Colesevelam in Subjects With Type 1 Diabetes Mellitus

Start date: July 2009
Phase: N/A
Study type: Interventional

This is a prospective, randomized, double blind, parallel, placebo controlled clinical trial evaluating the efficacy of colesevelam HCl in reducing LDL in subjects with type 1 diabetes mellitus over a 12 week treatment period. The aim is to highlight the effect of colesevelam on LDL cholesterol and glycemia in a type 1 diabetic population. The colesevelam group is anticipated to demonstrate a mean reduction in LDL by 10% compared to the placebo group, indicated by A1c and glycemic target range CGM readings.

NCT ID: NCT00934258 Available - Hyperlipidemia Clinical Trials

Effect of Genes on Rosuvastatin Therapy for Hyperlipidemia

Start date: n/a
Phase: N/A
Study type: Expanded Access

Previous studies indicate that the variant status of detoxification proteins is different among Taiwanese and other ethnic groups. For example, in Taiwanese, the major SNPs of CYP2C9 are CYP2C9*2 (430C>T) and CYP2C9*3 (1075A>C) and their frequencies are different from that in Caucasians [11]. The second example is that the frequency of the A(TA)7TAA allele in the promoter area of the UGT1A1 gene is substantially lower, while for the rate of variation within the coding region is much higher in Taiwanese than that in Caucasians (14.3% vs. 35.7- 41.5% and 29.3% vs. 0.1%, respectively) [12]. The third example is that the frequency of 388A>G of the OATP2 gene in Taiwanese (0.68) [13] is in between that in European Americans (0.30) and African Americans (0.74) [14]. Therefore, the investigators hypothesize that, in Taiwanese the SNPs of detoxification proteins modulate the lipid-lowing effects of RVA and fenofibrate may be different from those for Caucasians.

NCT ID: NCT00928616 Active, not recruiting - Hyperlipidemia Clinical Trials

Differential Effects of a Diet Supplementation With Plant Sterol Esters on Human Monocytes

PSE-MO
Start date: April 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the effects of a diet supplementation with plant sterol esters on serum lipids, plant sterol concentrations and monocyte subpopulations.

NCT ID: NCT00923676 Active, not recruiting - Hyperlipidemia Clinical Trials

Treatment of Hyperlipidemia and Sexual Dysfunction

Start date: April 2008
Phase: Phase 4
Study type: Interventional

Hyperlipidemias are frequently associated with and are considered an important cause of erectile dysfunction in men. This association has been attributed to the impairment of blood flow through endothelium-dependent relaxation in smooth muscle cells of corpus cavernosum. Basic science and human research suggest that the vascular pathophysiology of male and female sexual dysfunction may be similar, as the first phase of the female sexual response is mediated by a combination of vasocongestive and neuro-muscular event which include increased clitoral length and diameter, as well as increased vaginal lubrication, wall engorgement and luminal diameter. The investigators have shown that women with hyperlipidemia had a higher prevalence of sexual dysfunction as compared with age-matched women without hyperlipidemia. The aim of this study was to asses the effect of anti-hyperlipidemic drugs (fenofibrate and rosuvastatin, single or in combination) on validated indices of sexual function in hyperlipidemic men and women with sexual dysfunction at baseline.

NCT ID: NCT00917878 Completed - Inflammation Clinical Trials

Postprandial Effects of Milk and Milk Constituents

Start date: March 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether the addition of milk or the milk constituents calcium and protein to a high-fat breakfast affects the postprandial lipid and inflammatory response.

NCT ID: NCT00910988 Completed - Hyperlipidemia Clinical Trials

Healthy Volunteers Study of the Effects of Olanzapine and Ziprasidone

Start date: February 2009
Phase: N/A
Study type: Interventional

Primary Aim: To test the acute effects of olanzapine or ziprasidone administration, in comparison to placebo, on insulin sensitivity in antipsychotic-naïve healthy young men, measured as whole-body dextrose infusion rates (mg/kg/min), hepatic glucose production (glucose rate of appearance [Ra]), primarily muscle glucose utilization (glucose rate of disappearance [Rd]), and adipose tissue related free fatty acid production (glycerol rate of appearance [Ra]). We hypothesize that olanzapine, but not ziprasidone, will result in acute decreases in insulin sensitivity. Secondary Aim: To test the acute effects of olanzapine or ziprasidone on insulin signaling pathways in antipsychotic naïve healthy young men. We hypothesize that olanzapine, but not ziprasidone, will result in acute alterations in insulin signaling.

NCT ID: NCT00897975 Completed - Hyperlipidemia Clinical Trials

Red Yeast Rice and Phytosterols In Statin Intolerance

Start date: July 2009
Phase: Phase 2/Phase 3
Study type: Interventional

Red yeast rice may be useful to lower cholesterol, especially in a population of patients who cannot tolerate traditional therapy with statins. The addition of an over-the-counter phytosterol to red yeast rice may offer additional lipid lowering benefits when compared to red yeast rice alone. These supplements will be given to all participants. Up to one-half will enroll in a lifestyle intervention program called Change of Heart and will be compared to patients who do not participate in the program. The study will last one year.