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Prediabetic State clinical trials

View clinical trials related to Prediabetic State.

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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: NCT00763412 Completed - Clinical trials for Pancreatic Insufficiency

Pilot and Feasibility Study for the Treatment of Pre-diabetes in Patients With Cystic Fibrosis

Start date: November 2006
Phase: N/A
Study type: Interventional

The purpose of this study is to provide the necessary data and experience to design a larger, full scale clinical trial to determine if a certain medicine (repaglinide), which increases the amount of insulin secreted by the pancreas, can improve the nutritional status and pulmonary function of adolescents and young adults with cystic fibrosis and prediabetes by improving blood glucose control. The investigators are also trying to determine the relationship between systemic inflammatory factors and glucose impairment.

NCT ID: NCT00686816 Completed - Obesity Clinical Trials

Weight Loss in Pre-diabetic, Obese Women

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

This is a six (6) month, single center, randomized, double-blind, parallel, controlled-feeding weight-loss study comparing two dietary groups (triglyceride and olestra) in pre-diabetic obese women.

NCT ID: NCT00631345 Completed - Obesity Clinical Trials

Healthy Living Partnership to Prevent Diabetes

HELP PD
Start date: August 2007
Phase: N/A
Study type: Interventional

The Healthy Living Partnership to Prevent Diabetes (HELP PD) is a 300-participant randomized trial designed to test the effectiveness of a lay-health counselor led community-based diabetes prevention program in reducing blood glucose in people at risk for developing diabetes mellitus.

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: NCT00579813 Completed - Metabolic Syndrome Clinical Trials

Mechanisms Underlying Metabolic Syndrome in Obesity

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

The purpose of this study is to better understand the link between obesity and diabetes or pre-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: NCT00566319 Completed - Prediabetic State Clinical Trials

Can Structured Education Promote Physical Activity in Those Identified With an Increased Risk of Developing Diabetes

PREPARE
Start date: October 2006
Phase: N/A
Study type: Interventional

This study is a three-armed randomised controlled trial that aims to determine the effect of a structured educational programme on physical activity levels and glucose tolerance in individuals with impaired glucose tolerance (IGT). The educational programme is designed to promote physical activity by targeting perceptions and knowledge of IGT, exercise self-efficacy, and self-regulatory skills. The study will also investigate whether the effectiveness of the educational programme at promoting self-regulatory skills and physical activity is enhanced by the inclusion of a pedometer and personalised step/day goals.

NCT ID: NCT00561132 Completed - Prediabetic State Clinical Trials

Study of Vanadium Supplement in Patients With Impaired Glucose Tolerance

Start date: November 2003
Phase: Phase 3
Study type: Interventional

The purpose of this study was to evaluate if the vanadium can improve the insulin sensitivity in patients with impaired glucose tolerance. Secondary purpose of this study was to assess changes on metabolic profile, weight and blood pressure.

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.