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Metabolic Diseases clinical trials

View clinical trials related to Metabolic Diseases.

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NCT ID: NCT01731366 Active, not recruiting - Metabolic Disease Clinical Trials

The Effect of Whole Grain on Gut Microbiome and Metabolic Health

3G
Start date: August 2012
Phase: N/A
Study type: Interventional

Objective: To identify how specific changes of the whole grain content in the diet affect the host-gut microbiome interactions with implications for metabolic health . Design: A randomized, controlled, single-blinded, cross-over intervention trial consisting of two 8-week intervention periods, separated by a 6-week wash-out period. A total of 60 participants will be included. Intervention: low vs. high whole grain intake.

NCT ID: NCT01396954 Active, not recruiting - Clinical trials for Glucose Metabolism Disorders

Cirrhosis-Diabetes

CH-DM
Start date: November 2007
Phase: N/A
Study type: Observational

Glucose metabolism disorders (GMD) can be present in an overt and a subclinical way. They have negative impact in survival of patients with liver cirrhosis (LC). Their prevalence has not been determined in compensated cirrhotic patients.

NCT ID: NCT01367054 Active, not recruiting - Clinical trials for Nutritional and Metabolic Diseases

Adverse Events in Pharmaceutical Bioequivalence Study of Two Formulations of Metformine Hydrochloride 500 mg

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

The objective is evaluate, in healthy volunteers, the bioavailability of two products containing metformine 500 mg to determine if they are bioequivalent and identify the occurrence of adverse events.

NCT ID: NCT01174875 Active, not recruiting - Metabolic Diseases Clinical Trials

Growing Up in Singapore Towards Healthy Outcomes

GUSTO
Start date: June 2009
Phase:
Study type: Observational

This study aims to test the following hypotheses in women recruited in early pregnancy and whose children will be followed up till at least 14 years of age. - Epigenetic changes in conceptual tissues obtained at birth reflect the environment that the fetus was exposed to during development. - The pattern of epigenetic marks in gene promoters obtained from DNA in birth tissues, together with genotype, phenotype, and environmental exposures, can be utilized to assess how the perinatal environment affects subsequent metabolic, neurodevelopmental and other phenotypes.

NCT ID: NCT01028846 Active, not recruiting - Type 2 Diabetes Clinical Trials

Central Mechanisms That Regulate Glucose Metabolism in Humans

Start date: May 2011
Phase: Phase 4
Study type: Interventional

Type 2 diabetes is a chronic condition that affects the ability of the body to regulate glucose (sugar). When glucose levels are low, the liver can make glucose to increase levels in the body. This important process is called endogenous glucose production (EGP). Previous studies suggest that the central nervous system (CNS), including the brain, helps to coordinate this process by communicating with the liver through potassium channels. Control of EGP can be impaired in people with type 2 diabetes, which may contribute to the high levels of glucose seen in these individuals. The purpose of this study is to understand how activating these potassium channels in the control centers of the brain with a medication called diazoxide might inhibit the amount of glucose made by the liver. This is particularly important for people with diabetes who have very high production of glucose, which in turn causes hyperglycemia (high levels of sugar in the blood) that leads to diabetes complications.

NCT ID: NCT00119405 Active, not recruiting - HIV Infections Clinical Trials

Observational Study of Fat Loss in HIV Infected Adults Taking Nucleoside Reverse Transcriptase Inhibitors (NRTIs)

Start date: April 2005
Phase: Phase 2
Study type: Observational

Nucleoside reverse transcriptase inhibitors (NRTIs) are a class of anti-HIV drug that can be an important part of an HIV treatment regimen. Because anti-HIV therapy may have negative side effects, there is a great need to carefully study HIV infected patients on such regimens. One negative side effect observed in many HIV infected patients is lipoatrophy, a condition that results in fat loss in the body. It is unclear if NRTIs also have a role in the development of mitochondrial toxicity, a condition that affects the body's ability to produce energy. The purpose of this study is to observe the effects of an NRTI-based, protease inhibitor (PI)-sparing drug regimen on fat loss in HIV infected, treatment-naive adults. Study hypothesis: The initiation of NRTI-containing, PI-sparing therapy will inhibit mitochondrial DNA (mtDNA) synthesis and lead to a decrease in mtDNA content in adipose tissue, skeletal muscle and peripheral blood mononuclear cells (PBMCs), will cause deterioration in mitochondrial function, will increase fat apoptosis and oxidative damage biomarkers, and will lead to progressive decrease in body fat content.