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Pre-diabetes clinical trials

View clinical trials related to Pre-diabetes.

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NCT ID: NCT00842426 Completed - Obesity Clinical Trials

Evaluation of Lifestyle Interventions to Treat Elevated Cardiometabolic Risk in Primary Care

E-LITE
Start date: June 2009
Phase: Phase 2
Study type: Interventional

The purpose of the E-LITE Study is to evaluate the feasibility and potential effectiveness of two lifestyle interventions in a community based primary care setting. The study aims to assess how changes in diet, exercise, and behavioral self-management affect weight and related risk factors for adults at risk for diabetes and cardiovascular disease.

NCT ID: NCT00831129 Completed - Pre-diabetes Clinical Trials

A Study for Pre-diabetic Patients With Cholesterol Lowering Drugs

SIROCO
Start date: September 2006
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this research study is to examine if a combination of a cholesterol lowering-drug, simvastatin, with a sugar-lowering drug called rosiglitazone is more effective in improving vascular inflammation (irritation of the vessels that transport your blood) and other cardiovascular risk factors than the taking of simvastatin alone.

NCT ID: NCT00775684 Completed - Type 2 Diabetes Clinical Trials

Effect of Exenatide, Sitagliptin or Glimepiride on Functional ß -Cell Mass

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

This study evaluates exenatide, sitagliptin, and glimepiride for the treatment of high blood sugar in patients with impaired fasting glucose or early type 2 diabetes. The purpose of this study is to determine if exenatide and sitagliptin increase the amount of insulin made by the pancreas compared to glimepiride. It is hypothesized that exenatide or sitagliptin will sustain or increase the amount of insulin made by the pancreas in comparison to glimepiride.

NCT ID: NCT00707616 Completed - Pre-diabetes Clinical Trials

Common Genetic Variation and Type 2 Diabetes

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

Type 2 diabetes is a common metabolic disorder arising from a complex interaction between genetic predisposition and the environment. The development of this disorder is preceded by impaired glucose tolerance and elevated fasting glucose which also carry adverse cardiovascular risk. To date a few common genetic variants have been reliably associated with predisposition to type 2 diabetes. However, it is uncertain how these genes interact to alter insulin secretion and insulin action prior to the development of type 2 diabetes. We propose to utilize an established population-based cohort to determine how common genetic variants associated with type 2 diabetes alter the response to an oral glucose challenge in people without overt type 2 diabetes. This will enable us to understand how common variants alone or in combination alter whole-body glucose physiology and predispose to type 2 diabetes.

NCT ID: NCT00589459 Completed - Diabetes Clinical Trials

Gender Differences in Prevalence of Undiagnosed Diabetes in ACS

Start date: October 1, 2001
Phase:
Study type: Observational

The primary goal of this study is to measure the prevalence of undiagnosed pre-diabetes/diabetes among women hospitalized with acute coronary syndromes (ACS) compared to men. Inpatients with confirmed ACS (and no known prior history of diabetes) are invited to return to the Yale Hospital Research Unit 6-8 weeks after hospital discharge for an oral glucose tolerance test to identify individuals with pre-diabetes and diabetes.

NCT ID: NCT00570739 Completed - Clinical trials for Type 2 Diabetes Mellitus

Effects of Metformin Hydrochloride (HCl) in Combination With Colesevelam HCl, Compared to Metformin HCl Alone, in Patients With Type 2 Diabetes Mellitus and the Effects of Colesevelam HCl on Lipids and Glucose on Pre-diabetic Patients.

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

This is a 16-week double-blind, placebo-controlled (for colesevelam hydrochloride (HCl)) study in the type 2 diabetic subjects and pre-diabetic subjects. Diabetic participants will also be treated with open label, background,metformin HCl. Two-hundred sixty subjects with type 2 diabetes (T2DM) and 200 pre-diabetic subjects are planned to be be enrolled. Qualified subjects with T2DM will be randomized 1:1 to receive metformin HCl plus colesevelam HCl or metformin HCl plus placebo matching colesevelam HCl. Qualified pre-diabetic subjects will be randomized 1:1 to receive colesevelam HCl or matching placebo.

NCT ID: NCT00536250 Completed - Metabolic Syndrome Clinical Trials

Study to Investigate the Pathophysiology of Type 2 Diabetes in Youth

Start date: September 2001
Phase: N/A
Study type: Observational

The purpose of the study is to determine the role of beta-cell function and insulin resistance in the development of impaired glucose tolerance (IGT) and type 2 diabetes in children and adolescents who have an increased risk of developing type 2 diabetes due to overweight/obesity or a family history of overweight/obesity, diabetes and/or impaired fasting glucose. It is hypothesized that: 1)Obese adolescents with IGT will be more insulin resistant than obese adolescents with NGT. Insulin resistance will be the best predictor of changes in glucose tolerance status., 2)Beta cell function will be impaired in obese adolescents with IGT compared to obese adolescents with NGT., 3)Obese adolescents with IGT will present with greater intramyocellular, intrahepatic and visceral fat than obese adolescents with NGT. Furthermore, obese adolescents with IGT will have larger adipocytes, while having significantly fewer adipocytes compared to obese adolescents with NGT. Obese adolescents with IGT will also have altered expression of key genes related to insulin resistance., and 4)Abnormalities in endothelial function as manifested by low FMD and PAT are already present in obese adolescents with IGT and are linked to insulin resistance.

NCT ID: NCT00402194 Completed - Obesity Clinical Trials

Treating the Endothelium to Restore Insulin Sensitivity

Start date: June 2005
Phase: N/A
Study type: Interventional

A study of 12 weeks' treatment with losartan or placebo, to test the hypothesis that RAS inhibition will improve insulin' vascular actions and therefore improve insulin sensitivity in skeletal muscle.

NCT ID: NCT00384488 Completed - Pre-Diabetes Clinical Trials

Automated Diabetes Prevention Program

Start date: May 2004
Phase: N/A
Study type: Interventional

The objective for this pilot project is to determine the feasibility and effectiveness of the Interactive Voice Response protocol (IVR) on physical activity and eating behaviors in a group men and women who have been identified by their physician as being pre-diabetic. We hypothesize that participants receiving the IVR follow-up will have greater positive changes in their physical activity and eating behaviors when compared to those who receive only the standard-care pre-diabetes class.

NCT ID: NCT00364377 Completed - Pre-diabetes Clinical Trials

Incretins in Impaired Fasting Glucose

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

People with high fasting glucose can develop type 2 diabetes with the passage of time. This study is being done to determine the effect of a novel medication in people with this elevated fasting glucose. Sitagliptin is a substance that raises levels of a hormone normally found in the blood. This hormone, called glucagon-like peptide-1 (GLP-1), is normally released by the intestine in response to the presence of food. This hormone acts like a messenger between the intestine and the pancreas to raise insulin levels, and therefore, lower blood sugars. Sitagliptin is effective in people with diabetes, however, this study is being done to determine if Sitagliptin is effective in people with high fasting glucose who do not yet have diabetes.