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Hypertriglyceridemia clinical trials

View clinical trials related to Hypertriglyceridemia.

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NCT ID: NCT01242527 Completed - Clinical trials for Severe Hypertriglyceridemia

Epanova® for Lowering Very High Triglycerides

EVOLVE
Start date: January 2011
Phase: Phase 2/Phase 3
Study type: Interventional

The primary objective of the study is to determine the efficacy of Epanova (omefas) compared to placebo in lowering serum triglycerides in subjects with severe hypertriglyceridemia.

NCT ID: NCT01229566 Active, not recruiting - Clinical trials for Severe Hypertriglyceridemia

Efficacy Study to Treat Subjects With Severe Hypertriglyceridemia

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

The primary objective is to determine the efficacy of AKR963 compared to placebo and active comparator in lowering fasting triglyceride levels in patients with very high fasting triglyceride levels ≥ 500 and ≤ 1500 mg/dL.

NCT ID: NCT01211847 Completed - Dyslipidemia Clinical Trials

Efficacy Study of Diazoxide Choline to Treat Hypertriglyceridemia

Start date: October 2010
Phase: Phase 2
Study type: Interventional

Once a day oral administration with DCCR helps lower triglycerides

NCT ID: NCT01208961 Completed - Clinical trials for Severe Hypertriglyceridemia

Epanova® Compared to Lovaza® In a Pharmacokinetic, Single-dose, Evaluation

ECLIPSE
Start date: September 2010
Phase: Phase 2
Study type: Interventional

The objectives of this study are to compare the relative bioavailabilities of eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) in plasma from a single dose of Epanova or Lovaza during periods of high- and low -fat consumption.

NCT ID: NCT01182935 Completed - Type 2 Diabetes Clinical Trials

Elevated Triglyceride Levels and Later Type 2 Diabetes

Start date: April 2010
Phase: N/A
Study type: Observational

Subjects with elevated serum triglycerides in the 4th Tromso study in 1994/1995 were re-examined with an oral glucose tolerance test to see predictive value of triglycerides regarding development of type 2 diabetes

NCT ID: NCT01180764 Withdrawn - Clinical trials for Hypertriglyceridemia

Effects of Lovaza on High Density Lipoprotein (HDL) Composition and Function in Hypertriglyceridemia

Start date: August 2010
Phase: Phase 4
Study type: Interventional

Study hypothesis: Lovaza (purified prescription fish oil) is likely to help HDL (the "good cholesterol") work better. Study summary: We are testing effects of Lovaza versus placebo, on various aspects of HDL and other lipoproteins, in patients with high triglyceride levels. Study funding: This study is being funded by an investigator-initiated research grant from Glaxo Smith Kline.

NCT ID: NCT01150188 Completed - Clinical trials for Hypertriglyceridemia

Effects of Amino Acids on Regional Lipid Metabolism

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

Elevated fat level in blood is a risk factor for coronary heart disease, a major cause of death in America. The overall goal of this project is to test a novel treatment using nutrient (amino acid) supplementation against this condition in men and women, and to understand how this treatment works.

NCT ID: NCT01148004 Completed - HIV Clinical Trials

The Influence of Ritonavir, Alone and in Combination With Lopinavir, on Fenofibric Acid Pharmacokinetics in Healthy Volunteers

Start date: May 13, 2010
Phase: Phase 1
Study type: Interventional

Background: - Patients infected with the human immunodeficiency virus (HIV) are often treated with protease inhibitors that help fight HIV infection. However, these medications often increase blood cholesterol levels, particularly triglycerides and low-density lipoproteins, and can lead to heart disease and other problems. Patients may take drugs known as fibrates (such as gemfibrozil (Lopid )) to lower triglyceride levels, but even with maximum approved doses patients often cannot reach goal triglyceride levels. Research suggests that fibrates and certain HIV medications, such as ritonavir and lopinavir/ritonavir, may interact and decrease the effectiveness of the fibrate treatment. More research is needed to determine the best drug to lower triglyceride levels in HIV patients who are receiving protease inhibitor therapy. Objectives: - To evaluate the drug-drug interaction between fenofibrate and protease inhibitors lopinavir/ritonavir and ritonavir. Eligibility: - Healthy individuals between 18 and 60 years of age. Design: - This study will require a screening visit and 18 study visits. The screening visit will take 3 to 4 hours, and can occur 7 to 30 days before starting the study. The rest of the study, not including the screening visit, is 48 days. Three of the visits will take about 12 hours, and the remaining 15 visits will take about 1 hour. - For study days 1 to 7, participants will take fenofibrate alone. Participants will keep a daily record of medication doses and any side effects. - For study days 8 to 27, participants will take fenofibrate and ritonavir. Participants will keep a daily record of medication doses and any side effects. - For study days 29 to 48, participants will take fenofibrate and lopinavir/ritonavir. Participants will keep a daily record of medication doses and any side effects. - Participants will have regular study visits to provide blood samples for research and monitoring.

NCT ID: NCT01146522 Completed - Clinical trials for Hyperlipoproteinemia

Safety, Tolerability,Pharmacokinetics(PK)and Pharmacodynamics(PD)Assessment of LCQ908 in Patients With Severe Hypertriglyceridemia

Start date: May 2010
Phase: Phase 1/Phase 2
Study type: Interventional

This study will assess safety, tolerability, and effect of LCQ908 on blood lipids in patients with severe hypertriglyceridemia.

NCT ID: NCT01133210 Completed - Clinical trials for Hypertriglyceridemia

Effect of Maraviroc on Metabolic Function in Obese Subjects (Phase I)

Start date: January 2011
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine the effect of maraviroc therapy in obese insulin resistant subjects on: 1. Plasma triglyceride concentration 2. Plasma HDL-cholesterol and LDL-cholesterol concentrations 3. Plasma markers of cardiometabolic risk and inflammation