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Metabolic Syndrome X clinical trials

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NCT ID: NCT00632879 Recruiting - Insulin Resistance Clinical Trials

The Study of Metabolic Syndrome in Hemodialysis Patients

Start date: March 2007
Phase: N/A
Study type: Observational

Metabolic syndrome (MS), comprised of central obesity, glucose intolerance, hyperinsulinemia, low HDL-cholesterol (HDL-C), high triglyceride (TG) and hypertension, results in markedly increased risk for cardiovascular disease in the general population. The National Cholesterol Education Program Adult Treatment Panel III (NCEP ATP III) report recommended the use of five variables for the diagnosis of the MS including waist circumference (WC), serum TG concentration, serum HDL-C concentration, blood pressure and fasting glucose concentration. A waist circumference of 80 cm in women and 90 cm in men would better identify those with the MS in Asian populations. However, the studies of modified asian criteria of metabolic syndrome in hemodialysis (HD) patients are scarce. We will perform prevalence investigation, cross-sectional study, and prospective investigation for metabolic syndrome in our HD patients (around 360 at present). We will enroll all the patients who receive maintenance HD more than three months in our HD center. The patients who are hospitalizing, suffered from active malignancy, active infections, recent cardiovascular events and surgery will be excluded in the beginning of study. Biochemistry and anthropometric parameters including HDL-C, TG, insulin resistance index, high sensitivity C-reactive protein and WC will be collected and analyzed. We will also prospectively establish the mortality and hospitalization indices of these patients, to study the prognosis of HD patient with or without metabolic syndrome. This study will be helpful to understand whether the application of a modified criteria of metabolic syndrome in HD patients is capable to predict cardiovascular events, hospitalization and mortality rates.

NCT ID: NCT00632840 Completed - Obesity Clinical Trials

Pharmacological Regulation of Fat Transport in Metabolic Syndrome

Start date: June 2001
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether atorvastatin and fenofibrate are effective in the treatment of lipid disorders in obese, insulin resistant subjects.

NCT ID: NCT00631046 Completed - Obesity Clinical Trials

Essential Fatty Acids During Complementary Feeding

EFiON
Start date: February 2008
Phase: N/A
Study type: Interventional

The objective of this intervention study is to examine the effect of n-3 LCPUFA on growth and body composition, intestinal health and microbiotic composition, immune function and risk markers for later diseases in 9-18 months old infants and toddlers.

NCT ID: NCT00629213 Completed - Metabolic Syndrome Clinical Trials

Metabolic Syndrome Risk Factor in IGT: STOP-NIDDM Trial

Start date: n/a
Phase: Phase 3
Study type: Interventional

The aim of the study was to analyse the independent and joint effects of the components of the metabolic syndrome (MetS) on the incidence of diabetes in people with impaired glucose tolerance (IGT) and to assess the effect of acarbose by MetS status. Double-blind placebo controlled trial, 1,368 patients, follow-up time 3.3 years. MetS by ATP III definition with fasting plasma glucose of ≥ 6.1 mmol/l as limit for impaired fasting glucose (IFG).

NCT ID: NCT00628524 Completed - Clinical trials for Coronary Artery Disease

Homburg Cream & Sugar Study

HCS
Start date: February 2008
Phase: N/A
Study type: Observational

The purpose of this study is to prospectivly analyze the correlation of triglyceride tolerance and glucose tolerance with cardiovascular morbidity and mortality in patients with stable coronary artery disease within 18 months and to determine, whether measurement of triglyceride tolerance can discriminate patients at risk for cardiovascular events.

NCT ID: NCT00627757 Recruiting - Metabolic Syndrome Clinical Trials

Antipsychotic Medicine and Metabolic Syndrome

AMMS1
Start date: February 2008
Phase: N/A
Study type: Observational

The purpose of the study is to determine whether antipsychotic treatment is influence psychiatric patients due to endocrine and metabolic status and a quality of life. The investigators expect, that 30-50% of patients will show pharmacon - gene induced weight gain (> 7% of initial bodyweight) while the rest of patients will maintain unaltered bodyweight.

NCT ID: NCT00627380 Completed - Hypertension Clinical Trials

Yoga for the Management of HIV-Metabolic Syndromes

Start date: November 2005
Phase: Phase 4
Study type: Interventional

We are testing the safety and efficacy of a 16-wk yoga lifestyle intervention on oral glucose tolerance, fasting lipid/lipoprotein levels, body composition, cardiovascular function, quality of life, CD4+ T-cell counts and viral load in HIV-infected men and women with components of The Metabolic Syndrome. We hypothesize that a yoga lifestyle intervention will improve metabolic, anthropometric, cardiovascular disease parameters, and quality of life domains without adversely affecting immune or virologic status in people living with HIV.

NCT ID: NCT00621205 Completed - Metabolic Syndrome Clinical Trials

Gene Expression in Obesity and Insulin Resistance

Genobin
Start date: October 2003
Phase: N/A
Study type: Interventional

Lifestyle and genetic factors interact in the development of obesity and the metabolic syndrome. The molecular mechanisms underlying the beneficial dietary modifications are, however, unclear. We aimed to examine the effect of the long-term 30 moderate weight reduction on gene expression in adipose tissue (AT) and to identify genes and gene clusters responsive to treatment and thereby likely contributing to the development of the metabolic syndrome. Thus, randomized controlled and individualized weight reduction and physical exercise intervention was conducted. In the WR group, glucose metabolism improved that was not seen in other groups. Moreover, an inverse correlation between the change in SI and the change in body weight was found (r =-0.44, p=0.026). Down-regulation of gene expression (p<0.01) involving gene ontology groups of extracellular matrix, cell death was seen. Such changes did not occur in the other groups.

NCT ID: NCT00616057 Completed - Obesity Clinical Trials

Evaluation of Fructans Supplementation on Parameters of Metabolic Syndrome

FRUCTOB
Start date: February 2008
Phase: N/A
Study type: Interventional

Obesity is constantly increasing, causing an important risk to develop diseases such as heart disease, diabetes,... Some recent studies have shown that obese people present modifications of colon microflora and a low-grade inflammation. In our laboratory, we have demonstrated that the intake of fructans lessens dietary intake, body weight gain, adipose tissue accumulation and steatosis in rodents. These effects lead to an improvement of insulin resistance and hyperglycemia in diabetic rats and mice. Fructans are also able to restore the microflora disturbed by a high fat diet and to prevent endotoxemia. Moreover, studies have shown that fructans intake promotes satiety (Cani et al, Diabetes 2007) and or decreases fat mass (Abrams et al, Journal of Pediatrics 2007) in healthy human. An intervention study in obese patients is thus needed to study the effects of fructans in the target population.

NCT ID: NCT00614757 Suspended - Insulin Resistance Clinical Trials

Insulin Resistance Study

IR
Start date: May 2005
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate how often patients with hepatitis C infection have abnormalities of sugar and fat utilization. Additionally we would like to find out if these abnormalities of sugar and fat utilization are common in other liver diseases, or related to being overweight.