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Glucose Intolerance clinical trials

View clinical trials related to Glucose Intolerance.

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NCT ID: NCT01876992 Terminated - Obesity Clinical Trials

Metformin at the Cellular Level and Dosing for Diabetes Mellitus (DM)

Start date: January 2012
Phase: N/A
Study type: Interventional

The investigators know that metformin works at the level of the cells in the body by acting on a protein called Cyclic amine monophosphate- Response Binding Elements (CREB) binding protein or Constitutive Reverter of eIF2α Phosphorylation (CREP) Binding Protein (CBP). What the investigators do not know is how this process is affected when the dose of the metformin is increased or changed. Currently the same doses of metformin are often used in both children and adults, but it is possible that the dose of metformin should be based on age and weight. Understanding how CBP works could potentially help us to tailor metformin treatment individually for patients based on their age, weight and CBP response.

NCT ID: NCT01548651 Terminated - Clinical trials for Impaired Glucose Tolerance

Effect of Saxagliptin Treatment on Myocardial Fat Content, and Monocyte Inflammation

Start date: February 2012
Phase: Phase 4
Study type: Interventional

The purpose of the study is to examine the effect of saxagliptin, an anti-diabetes medication, on hepatic and myocardial fat content and monocyte inflammation in patients with Impaired Glucose Tolerance (IGT).

NCT ID: NCT01468376 Terminated - Clinical trials for Impaired Glucose Tolerance

GLU-xx Formulations in Individuals With Impaired Glucose Tolerance

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

The purpose of this study is to determine a safe,tolerable and efficacious dose of GLU-xx.

NCT ID: NCT01425424 Terminated - Prediabetes Clinical Trials

Prediabetes, Prehypertension and Vitamin D Supplementation - A Practice Based Clinical Intervention Pilot Study

Start date: April 2012
Phase: N/A
Study type: Interventional

This randomized, double-blind, placebo-controlled, multi-site study is to reverse modest elevations of fasting blood sugar (prediabetes) and resting blood pressure(Prehypertension) or both co existing prediabetes and prehypertension by increasing blood levels of vitamin D. This may reduce the chances of developing diabetes or high blood pressure or both later in life.

NCT ID: NCT01017263 Terminated - Obesity Clinical Trials

Vyvanse and Glucose Intolerance in Children With Attention Deficit Hyperactivity Disorder (ADHD) and Obesity

Start date: December 2009
Phase: Phase 4
Study type: Interventional

The purpose of this study to assess the effects of chronic administration of Vyvanse (lis-dexamphetamine) on glucose metabolism in a sample of children and adolescents with Attention Deficit Hyperactivity Disorder (ADHD) who also have glucose intolerance and are obese.

NCT ID: NCT00846521 Terminated - Clinical trials for Cardiovascular Disease

Study of Post-meal Blood Sugar Peaks in Association With Vascular Disease in Childhood Obesity

Start date: September 2006
Phase: Phase 4
Study type: Interventional

The main purpose of this study is to determine whether treatment with acarbose attenuates post-prandial glycemic excursions in non-diabetic/pre-diabetic obese children as determined by continuous glucose monitoring systems (CGMS). To this effect the current pilot study involves a 6 week intervention with acarbose given to all subjects with either impaired glucose tolerance or an area under the curve of >130 mg/dl during the screening oral glucose tolerance test. Three consecutive days of CGMS are then compared to before and during the intervention. The secondary objective addressed in this protocol is the collection of baseline measures of endothelial function in obese and lean children. Even though the duration of acarbose treatment may be too short to demonstrate a vascular effect, the pre and post intervention data would serve as preliminary data for anticipated future studies that assess the vascular effect of reduced post-prandial blood glucose levels.

NCT ID: NCT00837590 Terminated - Obesity Clinical Trials

Vascular Function, Endothelin, and Inflammation in Pre-diabetic Obesity Versus Lean Healthy Controls

Start date: March 2009
Phase: Phase 1
Study type: Interventional

Aims: 1. Does inflammation contribute importantly to concurrent defects in vascular and metabolic dysfunction in human pre-diabetic obesity? 2. Are there benefits of anti-inflammatory treatment strategies in pre-diabetic obesity in the context of existing treatment with metformin? 3. Are there benefits of anti-inflammatory treatment strategies in pre-diabetic obesity in the context of existing treatment with lisinopril?

NCT ID: NCT00554112 Terminated - Aging Clinical Trials

Regulation of B-Cell Function & Glucose Tolerance in Older People

Start date: November 2007
Phase: N/A
Study type: Interventional

This VA CDA-2 proposal will test in detail if lifestyle intervention with aerobic exercise training improves the body's production of insulin in older people at risk to develop diabetes.

NCT ID: NCT00510705 Terminated - Obesity Clinical Trials

Chronic Inflammatory Activation in Fat Tissue: An Atherogenic Factor in Severe Coronary Artery Disease

KFO
Start date: July 2007
Phase: N/A
Study type: Interventional

Chronic inflammatory activation in fat tissue can be the link between adiposity and an increased risk for atherosclerosis. The aim of this study is to investigate how molecular alterations in fat tissue can be influenced by regular physical exercise training alone or in combination with a medical therapy (glitazone or metformin) in obese patients with severe coronary artery disease (CAD) and impaired glucose tolerance.

NCT ID: NCT00325650 Terminated - Prediabetic State Clinical Trials

Rimonabant In Prediabetic Subjects To Delay Onset Of Type 2 Diabetes (RAPSODI)

Start date: May 2006
Phase: Phase 3
Study type: Interventional

Primary: effect of long-term administration on the time of progression to type 2 diabetes in patients with prediabetes (i.e., Impaired Fasting Glucose (IFG) or Impaired Glucose Tolerance (IGT) or both at baseline). Secondary: Effect on weight loss and weight maintenance, sustained effect of rimonabant following a washout period, other markers of glycemic control (fasting glucose, fasting-insulin and HbA1c), glucose tolerance and insulin responses during OGTTs, other risk factors (HDL-Cholesterol, TG), quality of life - Safety and tolerability.