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Prediabetic State clinical trials

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NCT ID: NCT02167620 Completed - Clinical trials for Diabetes Mellitus, Type 2

Metformin in Co-morbid Diabetes or Prediabetes and Serious Mental Illness

Start date: June 2014
Phase: Phase 4
Study type: Interventional

Schizophrenia is associated with a lifespan shortened by 20 years, due to cardiovascular disease (CVD), with antipsychotic (AP) medications understood to contribute to this risk through associated metabolic side-effects. Metformin, a medication used to treat prediabetes, and diabetes in the general population, holds promise with regard to reduction of AP-related metabolic problems, but has not been directly tested in early episode patients beyond weight loss, nor specifically in patients with diabetes or prediabetes and psychosis. We propose to replicate findings that metformin can reduce weight gain, and dysglycemia uniquely focusing on an early episode population diagnosed with prediabetes or diabetes. To help determine long-term risk/benefit of adjunctive metformin, we propose to look at changes in abdominal and liver fat, two well-established risk factors for CVD. Given links between dysglycemia, obesity with hippocampal volume loss and cognitive dysfunction, we will explore if improvements in metabolic indices are associated in changes in cognition and brain structure.

NCT ID: NCT02140983 Completed - Dementia Clinical Trials

Effects of Liraglutide on Hippocampal Structure and Function in Aging Adults With Prediabetes

LGT
Start date: August 2013
Phase: Phase 1
Study type: Interventional

The purpose of this study is to evaluate the effects of liraglutide on the memory and attention of people with insulin resistance. Liraglutide is a medication that makes the body more sensitive to insulin, and therefore may allow it to manage sugar more effectively. The investigators are looking specifically at a region of the brain that is associated with memory and attention, called the hippocampus, in order to see whether treatment this treatment will change performance on memory and attention tasks. The investigators are also taking an MRI of the brain to see whether there are changes to the size and shape of the hippocampus after treatment. All subjects in this study will be 50-70 years old and have pre- diabetes. Half of all subjects will have a family history of dementia, while the other half will not.

NCT ID: NCT02129595 Completed - Pre-diabetes Clinical Trials

Resveratrol and First-degree Relatives of Type 2 Diabetic Patients

Start date: April 2014
Phase: N/A
Study type: Interventional

The main objective of the study is to investigate if resveratrol supplementation can improve overall and muscle-specific insulin sensitivity in first-degree relatives of type 2 diabetic patients. As a secondary objective the investigators want to investigate whether the improved insulin sensitivity can be attributed to improved muscle mitochondrial oxidative capacity and a reduced intrahepatic and cardiac lipid content. Furthermore, in a subset of the participants the investigators want to investigate the effect of resveratrol on glucose uptake in brown adipose tissue.

NCT ID: NCT02124590 Completed - Elderly Clinical Trials

The Effect of Oral Carnitine Supplementation on MRS-derived Mitochondrial Function

Start date: June 2014
Phase: N/A
Study type: Interventional

This is a longitudinal study supported by Pfizer and is a collaboration between DMPI (Duke Molecular Physiology Institute) and DIAL (Duke Image Acquisition Laboratory) to measure the effects of acute exercise on carnitine and acylcarnitine levels in the muscle and on insulin sensitivity in the plasma. This pilot study seeks to explain why moderate intensity exercise provides more improvements in glucose control for pre-diabetic patients than vigorous intensity. The investigators hypothesize that moderate intensity exercise might be beneficial for elderly individuals who are overweight or obese, specifically by: 1. Reducing damaging excess protein acetylation (measured in muscle biopsy), 2. Improving the acylcarnitine/carnitine ratio (measured by MRS), 3. Improving overall mitochondrial function as reflected in reduced phosphocreatine recovery time (measured by MRS) and 4. Increasing insulin sensitivity as measured by a 4-hour oral glucose tolerance test. Investigators intend to use the results of this study to show feasibility in measuring mitochondrial function at Duke for a larger federal grant submission. Investigators hypothesize that carnitine insufficiency might contribute to mitochondrial dysfunction and obesity-related impairments in glucose tolerance and insulin action.

NCT ID: NCT02119325 Completed - Clinical trials for Impaired Fasting Glucose

The Effect of a Nutritional Supplement on Post Prandial Glucose and Lipids in an Adult Population

Start date: September 2013
Phase: N/A
Study type: Interventional

The primary aim of this study is to evaluate the effect of a fibre rich health food drink on the post prandial glucose and triglyceride peak in healthy overweight adults with impaired fasting glucose (IFG). The study is randomised, stratified, double blind, two treatments, two period cross over study.

NCT ID: NCT02104739 Completed - Obesity Clinical Trials

Effects of Antidiabetic Medications on the Postprandial State in Prediabetes

Start date: April 2014
Phase: Phase 4
Study type: Interventional

This project addresses cardiovascular disease risk in patients with prediabetes. Levels of lipids after eating a meal ("postprandial lipids") are strong independent predictors of cardiovascular risk. Newer anti-diabetic agents - exenatide and saxagliptin - impact lipid metabolism. These medications will be studied for their effect in reducing both postprandial lipid levels and arterial dysfunction.

NCT ID: NCT02084654 Completed - Insulin Resistance Clinical Trials

Exenatide and Weight Loss for Diabetes Prevention

Start date: November 2007
Phase: Phase 1
Study type: Interventional

Exenatide, a GLP-1 agonist approved for lowering blood glucose concentrations in patients with type 2 diabetes, has been associated with restoration of the first-phase insulin response when administered intravenously to patients with type 2 diabetes. In longer clinical trials, it is associated with progressive decreases in body weight, and improvement in the dyslipidemia that characterizes insulin resistance, although insulin resistance was not quantified. The investigators will seek to determine whether exenatide would have similar effects in individuals who were not diabetic. in particular, the drug effect on beta cell function and insulin sensitivity would be subject to less confounding by changes in blood glucose in the prediabetic population, allowing for clearer evaluation of the physiological effects of the drug on these metabolic endpoints. The investigators will compare 2 groups of prediabetic insulin resistant individuals, all on a weight loss diet and one group on exenatide and the other on placebo. The investigators will evaluate restoration of first phase insulin response, potential glucose lowering effects, including both reversal of prediabetes and hypoglycemia, and improvement in insulin resistance.

NCT ID: NCT02063048 Completed - Prediabetes Clinical Trials

Text Messaging for Weight Loss

Start date: April 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the effectiveness of text message-based support to usual care at promoting weight loss in patients with pre-diabetes.

NCT ID: NCT02060240 Completed - Obesity Clinical Trials

Physical Activity and Obesity

Start date: February 2014
Phase: N/A
Study type: Interventional

The purpose of the study is to see if a twelve-week exercise intervention in overweight or obese subjects with pre-diabetes or early disease course type 2 diabetes can lead to improved skeletal muscle capillary blood flow by improving substances that dilate blood vessels and result in improved insulin sensitivity.

NCT ID: NCT02043405 Completed - Diabetes Clinical Trials

Weight Loss and/or Exercise Training to Discover Muscle Lipids Related to Insulin Sensitivity

Start date: January 2014
Phase: N/A
Study type: Interventional

The investigators will use exercise training and weight loss to discover localized lipid species related to diabetes risk in people.