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Prediabetic State clinical trials

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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.

NCT ID: NCT00480779 Completed - Metabolic Syndrome Clinical Trials

Evaluation of Group Lifestyle Balance DVD in Primary Care Practice

STEP UP
Start date: June 2007
Phase: N/A
Study type: Interventional

The purpose of this study is to examine different ways of delivering the Group Lifestyle Balance (GLB) intervention (1). The GLB is a 12-week lifestyle change program based on the highly successful lifestyle program that was used in the Diabetes Prevention Program (DPP)(2). A DVD of the Group Lifestyle Program has been developed. Conditions called metabolic syndrome and pre-diabetes increase the risk of diabetes and heart disease. Recent research has shown that type 2 diabetes and metabolic syndrome may be prevented or delayed by making lifestyle changes. Two local primary care practices will be randomly assigned to either the GLB-DVD intervention or usual care. Two additional practices will provide the GLB using trained preventionists for delivery. Approximately 15 patients will be recruited in each practice. It is not known if the GLB intervention works better than what is usually done at the present time for people with metabolic syndrome or pre-diabetes. It is hoped that this research study will provide information to help answer that question.

NCT ID: NCT00455403 Completed - Hypertension Clinical Trials

Atheroma Reduction With Chloroquine in Patients With the Metabolic Syndrome (ARCH-MS)

ARCH-MS
Start date: April 2006
Phase: N/A
Study type: Interventional

Metabolic syndrome consists of a group of co-occuring conditions that increase an individual's risk of developing heart disease, stroke, and diabetes. The purpose of this study is to evaluate the long-term effectiveness of chloroquine, a protein-activation medication, at reducing the progression of atherosclerosis in patients with the metabolic syndrome. Sub-study: Vascular endothelial growth factor(VEGF)and Cardiometabolic Risk, The purpose is to determine if the association of VEGF with atherosclerosis indicates that it should be a marker of the disorder.

NCT ID: NCT00455325 Completed - Hypertension Clinical Trials

Chloroquine to Treat People With Metabolic Syndrome Aim2 (ARCH-MS)

ARCH-MS
Start date: September 2004
Phase: Phase 2
Study type: Interventional

Metabolic syndrome consists of a group of co-occuring conditions that increase an individual's risk of developing heart disease, stroke, and diabetes. The purpose of this study is to evaluate the short-term effectiveness of chloroquine, a protein-activation medication, at improving metabolic syndrome.

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: NCT00358254 Completed - Clinical trials for Diabetes Mellitus, Type 2

Noninvasive Skin Spectroscopy for Diabetes Screening

Start date: October 2004
Phase: Phase 1
Study type: Observational

The objective of this study is to assess the performance of a noninvasive device for the early screening of Diabetes Mellitus.