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Insulin Resistance clinical trials

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NCT ID: NCT00656851 Completed - HIV Infections Clinical Trials

Myocardial Function & FFA Metabolism in HIV Metabolic Syndrome

WU197
Start date: September 2005
Phase: N/A
Study type: Interventional

We hypothesize that the hearts of HIV+ people with The Metabolic Syndrome use and oxidize fats and sugars inappropriately, and that this may impair the heart's ability to pump blood. We hypothesize that exercise training or pioglitazone (Actos) will improve fat and sugar metabolism in the hearts of HIV+ people with The Metabolic Syndrome. This study will advance our understanding of cardiovascular disease in HIV+ people, and will test the efficacy of exercise training and pioglitazone for improving insulin resistance, heart metabolism and heart function in this at risk population.

NCT ID: NCT00656032 Completed - Clinical trials for End Stage Renal Disease

Vitamin D, Insulin Resistance and Inflammation in ESRD

Start date: April 2008
Phase: Phase 2
Study type: Interventional

The broad goal of this study is to understand the mechanisms by which Vitamin D receptor activation leads to changes in insulin signaling in advanced uremia. We hypothesize that 1,25-Dihydroxyvitamin D3 deficiency due to advanced chronic kidney disease leads to insulin resistance and that administration of a vitamin D3 analog will restore insulin sensitivity in End Stage Renal Disease patients.

NCT ID: NCT00655018 Completed - Inflammation Clinical Trials

Effect of Vitamin E on Pediatric Nonalcoholic Fatty Liver Disease (NAFLD)

VITENAFLD
Start date: January 2003
Phase: Phase 2/Phase 3
Study type: Interventional

No proven treatment exists for nonalcoholic fatty liver disease (NAFLD) in children and adolescents. We aim to determine the efficacy of lifestyle intervention with or without antioxidant therapy in pediatric NAFLD.

NCT ID: NCT00654667 Withdrawn - Insulin Resistance Clinical Trials

Mechanisms of Metabolic Regulation of Resveratrol on Humans With Metabolic Syndrome

RSV
Start date: May 2007
Phase: Phase 2
Study type: Interventional

Sirtuin activators may prove useful in treating age-related diseases and extending lifespan in humans. Resveratrol (RSV), a polyphenol found in red wine, has been shown in vitro to enhance SIRT1 activity. RSV is associated with some of the beneficial effects of red wine or the "French Paradox". Recently RSV has been associated with increasing lifespan in mice on a high calorie diet and improved metabolic profile and activity levels. The effect of this small molecule in humans is unknown. Preclinical observations suggest that RSV is safe and has enormous potential in the treatment of obesity and insulin resistance in humans. This pilot study will examine the effect of RSV on improving the metabolic profile of adults with insulin resistance. Specifically, this randomized double blind placebo controlled study will examine the effects of 4 weeks of supplementation with RSV 5.0 grams daily, compared to placebo control (PC) on the metabolic profile of 36 men and women over the age of 50 with insulin resistance (IR) consuming a typical western diet consisting of at least 40% calories from fat.

NCT ID: NCT00654056 Completed - Clinical trials for Type 2 Diabetes Mellitus

Severe Insulin Resistance in Patients With Type 2 Diabetes

Start date: March 2008
Phase: N/A
Study type: Interventional

The purpose of the study is to investigate some of the mechanisms behind severe insulin resistance and to determine the dose response to insulin in patients with type 2 diabetes mellitus.

NCT ID: NCT00652379 Completed - Insulin Resistance Clinical Trials

Co-treatment With Pegvisomant and a Somatostatin Analogue (SA) in SA-responsive Acromegalic Patients

Start date: June 2008
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate if co-treatment of acromegalic patients, who beforehand are considered well-controlled on SA monotherapy, with pegvisomant and SA will improve insulin sensitivity and glucose tolerance, and if these effects of co-treatment can be obtained at a neutral cost as compared to SA mono therapy. Second to investigate body composition, substrate metabolism, symptoms, intrahepatic and intramyocellular fat.

NCT ID: NCT00647179 Completed - Insulin Resistance Clinical Trials

Substrate Metabolism and Insulin Sensitivity in Acromegalic Patients Before and After Treatment

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

The purpose of this study is to investigate the effects of chronic elevated growth hormone on metabolism and insulin sensitivity by studying acromegalic patients before and after treatment.

NCT ID: NCT00646815 Completed - Clinical trials for Growth Hormone Deficiency

Insulin Sensitivity and Substrate Metabolism Before and After Treatment in Patients With Growth Hormone Deficiency

Start date: March 2008
Phase: N/A
Study type: Interventional

The purpose of this study is to further characterize the treatment related changes in insulin sensitivity, substrate metabolism and intrahepatic-intramyocellular lipids in patients with growth hormone deficiency (GHD).

NCT ID: NCT00646698 Completed - Obesity Clinical Trials

Body Composition and Very-Low-Density-Lipoprotein-Triglycerides (VLDL-TG) Kinetics

Start date: April 2006
Phase: N/A
Study type: Observational

Context: Upper body obese (UBO) subjects are more likely to develop cardiovascular disease (CVD) than lower body obese (LBO) or lean. This may in part be caused by greater hepatic secretion of very-low-density-lipoprotein-triglycerides (VLDL-TG). Objective: To assess the impact of body composition and insulin sensitivity on basal VLDL-TG turnover in women.

NCT ID: NCT00644475 Recruiting - Clinical trials for Essential Hypertension

Imidapril and Candesartan on Fibrinolysis and Insulin-Sensitivity in Patients With Mild to Moderate Hypertension

Start date: March 2008
Phase: Phase 3
Study type: Interventional

BACKGROUND The effects of ACE-inhibitors on fibrinolysis are well documented. Experimental and clinical studies have shown that ACE inhibitors induce a reduction in plasma PAI-1 levels in many cardiovascular diseases, like hypertension, coronary heart disease, and heart failure. Their effects on t-PA are more controversial, due to the fact that t-PA exists in several forms, including free and bound to PAI-1. Indeed an increase in t-PA activity has been observed in humans and it seems related to bradykinin increase which is known to stimulate endothelial t-PA synthesis. These favourable effects on fibrinolysis could be related not only to the Angiotensin II reduction and the bradykinin increase but also to the improvement in insulin sensitivity, as insulin has been suggested as one of the main regulators of fibrinolytic activity. To date conflicting results have been reported about the effects of ARBs on fibrinolysis. Some studies have reported small improvements, others no significant effect. These conflicting results may be due to possible methodological bias but a possible pathophysiological explanation might be that receptor subtypes other than AT1 mediate the effect of Angiotensin-II on endothelial PAI-1 expression, i.e. the AT4 receptors, and during AT1 receptor blockade there is an important increase not only of Angiotensin-II, but also of all its catabolites including Angiotensin IV. The dissimilar effects on of ACE Is and ARBs may also depend on their different action on the RAS and their different effect on insulin sensitivity: ACE-Is improve insulin sensitivity, while the majority of ARBs have been reported to have a neutral effect. Moreover, unlike ACE-Is, ARBs do not affect the metabolism of bradykinin, which is known to stimulate t-PA synthesis and release. AIM OF THE STUDY The aim of this study is to verify the effect of imidapril compared to candesartan on insulin sensitivity, evaluated through the euglycemic hyperinsulinemic clamp, and on fibrinolysis, evaluated through the plasma PAI-1 and t-PA activity, in mild to moderate hypertensive patients.