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Metabolic Syndrome clinical trials

View clinical trials related to Metabolic Syndrome.

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NCT ID: NCT01123278 Completed - Obesity Clinical Trials

Testosterone Replacement in Metabolic Syndrome and Inflammation

TERMSINFAT
Start date: January 2004
Phase: Phase 4
Study type: Interventional

Hypogonadism (HG) frequently complicates the Metabolic Syndrome (MetS), whether testosterone replacement (TRT) is beneficial has not been clearly ascertained. This study was designed to address the effects of TRT on insulin resistance, body composition and pro-inflammatory status in naïve patients with MetS and HG.

NCT ID: NCT01120873 Completed - Metabolic Syndrome Clinical Trials

The Effect of Metamin 3D on the Lipid and Glucose in Subjects With Metabolic Syndrome

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

To evaluate the effect of Metamin 3D on improvement of glucose and lipid on Taiwanese subjects with metabolic syndrome.

NCT ID: NCT01119989 Completed - Metabolic Syndrome Clinical Trials

Effects of an Amino-acid Supplement on Hepatic Lipid Metabolism

AMINOFRUCT
Start date: May 2010
Phase: N/A
Study type: Interventional

10 healthy male volunteers will be studied after - a 6 day weight maintenance, balanced diet - a 6 days weight maintenance, balanced diet supplemented with 3 grams fructose/kg body weight/day - a 6 days weight maintenance, balanced diet supplemented with 3 grams fructose/kg body weight/day and 20g amino-acids per day At the end of each 6 days period, the following measurements will be obtained - intrahepatic lipids (1H-MRS) - metabolic effects of fructose ingestion (measurement of substrate oxidation, gluconeogenesis from fructose, palmitate synthesis from fructose, plasma VLDL-kinetics) This is a randomized, double blinded study

NCT ID: NCT01119690 Completed - Metabolic Syndrome Clinical Trials

Hämeenlinna Metabolic Syndrome Research Program: Effects of Rapeseed Oil on Serum Lipids and Platelet Function

HMS-03
Start date: September 2004
Phase: N/A
Study type: Interventional

In this study, the effects of dietary intake of cold-pressed turnip rapeseed oil (CTPRO) and milk fat are compared in men with metabolic syndrome having already participated in HMS-02 study.

NCT ID: NCT01114763 Completed - Metabolic Syndrome Clinical Trials

Hämeenlinna Metabolic Syndrome Research Program: Oxidized LDL and Arterial Elasticity in Metabolic Syndrome and Controls (HMS-01)

HMS-01
Start date: June 2003
Phase: N/A
Study type: Observational

Mechanisms that link metabolic syndrome to atherosclerosis are incompletely understood. As a part of Hämeenlinna Metabolic Syndrome Research Program (HMS), 40 men with metabolic syndrome and their 40 physically active controls (age: 30 to 65 years) are compared in a cross-sectional study. Except routine laboratory parameters, arterial elasticity and levels of oxidized LDL are determined. Study hypothesis: Levels of oxidized LDL and findings in arterial elasticity may differ between subjects with metabolic syndrome and controls explaining the elevated risk for cardiovascular diseases among patients with metabolic syndrome.

NCT ID: NCT01103921 Completed - Metabolic Syndrome Clinical Trials

The Metabolic Effects of Consuming Sugar-Sweetened Beverages for Two Weeks

DRS
Start date: October 2008
Phase: N/A
Study type: Interventional

The purpose of this study is to examine the effects of consumption of sugar-sweetened beverages on blood triglycerides and cholesterol, cholesterol concentrations, and the body's sensitivity to insulin.

NCT ID: NCT01099306 Completed - Metabolic Syndrome Clinical Trials

Pharmacist - Physician Collaborative Approach to the Management of Metabolic Syndrome

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

This study devised an experimental focused pharmaceutical care program, allowed a clinical pharmacist to work in a physician office to assess and manage patients' metabolic syndrome status and its individual components. This study described the clinical benefits of physician- clinical pharmacist interaction in achieving improved glycemic control, lipid and blood pressure measurements, involving medication, diet, physical activity and patient heath care counseling.

NCT ID: NCT01094158 Completed - Metabolic Syndrome Clinical Trials

Study of Aramchol in Patients With Fatty Liver Disease or Nonalcoholic Steatohepatitis

Aramchol003
Start date: November 2010
Phase: Phase 2
Study type: Interventional

Primary purpose: Compare the changes in liver triglycerides concentration in the Aramchol versus the placebo arm following three month treatment. Secondary purpose: Comparing liver enzymes, markers of endothelial dysfunction, insulin resistance, SCD1 activity and cholesterol synthesis and lipid levels, between the Aramchol and the placebo arms.

NCT ID: NCT01087632 Completed - Metabolic Syndrome Clinical Trials

Armolipid Plus and Metabolic Syndrome

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

Metabolic syndrome is a highly prevalent condition characterized by visceral obesity, abnormalities of glucidic and lipid metabolism, and increased risk for cardiovascular events. Such findings appear to be associated with a decrease in insulin sensitivity. Management of metabolic syndrome is currently aimed at treating individual components of the disease without addressing this underlying pathophysiologic mechanism; this translates into multidrug regimens, high costs and patient compliance issues. Armolipid Plus (an association of berberine 500 mg, red yeast rice titled in 3 mg monacolin K,policosanol 10 mg,coenzyme Q10 2 mg,astaxanthin 0,5 mg,folic acid 0,2 mg) has been found to be effective at reducing blood cholesterol and triglycerides, and at improving endothelial function; subgroup analyses also suggested a benefit on indices of insulin resistance. Aim of the study is to evaluate the effects of Armolipid Plus on insulin sensitivity and on the diagnostic parameters of metabolic syndrome. 60 patients will be enrolled in this randomized, double-blind, placebo-controlled trial; active treatment will consist of Armolipid Plus (1 tbl qd). Primary end point will be the reduction of the insulin/glucose ratio, both after overnight fast (HOMA index) and after an oral glucose tolerance test (OGTT).

NCT ID: NCT01087086 Completed - Obesity Clinical Trials

Reduction of the Metabolic Syndrome in Navarra-Spain

RESMENA-S
Start date: January 2010
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether a dietary pattern based on crononutrition and dietary training, together with dietary and psychological control, can reduce the body weight, improve the oxidative and inflammatory state in subjects with diagnosed metabolic syndrome features and can reduce the prevalence of the Metabolic syndrome in the population.