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Impaired Glucose Tolerance clinical trials

View clinical trials related to Impaired Glucose Tolerance.

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NCT ID: NCT02621060 Completed - Clinical trials for Impaired Glucose Tolerance

Effect of Chlorogenic Acid on Patients With Impaired Glucose Tolerance

Start date: September 2015
Phase: Phase 2
Study type: Interventional

Chlorogenic acid has demonstrated promising effects in the treatment of glycemic control, obesity, dyslipidemia, insulin secretion, among others. The above mentioned findings show that Chlorogenic acid has an excellent potential for the control of glucose as well as insulin secretion and insulin sensitivity.

NCT ID: NCT02569762 Completed - Clinical trials for Impaired Glucose Tolerance

Effects of Artificial Sweeteners on Gut Microbiota and Glucose Metabolism

Start date: July 2016
Phase: N/A
Study type: Interventional

The Objectives of this study is to determine the effect(s) of daily non-caloric artificial sweetener (NAS) consumption (sucralose or aspartame) on the composition of the bacteria and also to determine the changes in glucose metabolism.

NCT ID: NCT02455934 Completed - Clinical trials for Impaired Glucose Tolerance

Effects of D-allulose (Psicose) With Sucrose Beverage on Glucose Tolerance and Insulin Level

Start date: April 2015
Phase: N/A
Study type: Interventional

Randomized, double-blind, crossover-trial, 30 subjects in each groups, either males or females, normal fasting glucose or pre-diabetes, aged > 18 years old to perform oral sucrose tolerance with either one of the 5 study products 1. Sucrose 50 g 2. Sucrose 50 g + D-allulose (psicose) 2.5 g 3. Sucrose 50 g + D-allulose (psicose) 5 g 4. Sucrose 50 g + D-allulose (psicose) 7.5 g 5. Sucrose 50 g + D-allulose (psicose) 10 g Primary endpoints: 1. To investigate the dose-response effects of D- allulose (psicose) with sucrose beverage on glucose tolerance 2. To investigate the dose-response effects of D- allulose (psicose) with sucrose beverage on insulin levels

NCT ID: NCT02254317 Completed - Clinical trials for Impaired Glucose Tolerance

Dose-dependent Effect of Grape Seed Extract on Glucose Control in People With Impaired Glucose Tolerance

GSE3
Start date: September 15, 2014
Phase: N/A
Study type: Interventional

The objective is to identify the lowest effective dose of Grape Seed Extract (GSE) on glucose control in people with impaired glucose tolerance (IGT).

NCT ID: NCT02248272 Completed - Hyperglycemia Clinical Trials

Effect of Meal Frequency on Glycemic Control of People at High Risk or Diagnosed With Diabetes

Start date: October 2011
Phase: N/A
Study type: Interventional

This study investigated any potential associations between two isocaloric diets with different meal frequency (3 meals versus 6 meals) and glycemic control in people at high diabetes risk (lean and overweight/obese women with PCOS, individuals with hyperinsulinemia, individuals with impaired glucose tolerance) and diagnosed with diabetes.

NCT ID: NCT02158481 Completed - Vascular Diseases Clinical Trials

Effects of Dietary Ingredients on Vascular Function

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

The main aim of the study is to investigate the effects of dietary ingredients (polyphenols and carotenoids) on vascular function during acute glucose load. Each subject will receive 4 weeks of intervention with test product or placebo product after a dietary restriction run-in period of 14 days. Subjects will be challenged with an oral glucose tolerance test (OGTT) immediately after the run-in phase and at the end of the intervention phase. During the OGTT, blood samples will be taken at regular intervals. The study will be conducted in subjects with impaired glucose tolerance.

NCT ID: NCT02151188 Completed - Obesity Clinical Trials

Liquid Protein Preloads With Different Carbohydrate Types Effects on the Glycaemic and Insulinaemic Response

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

This study hypothesizes that milk protein consumed together or shortly before a white rice or white bread carbohydrate meal exerts different influence on the glycaemic, insulinaemic responses.

NCT ID: NCT02135172 Completed - Clinical trials for Impaired Glucose Tolerance

Breaks in Sedentary Time and Glucose Regulation in Women

ACUTE
Start date: October 2013
Phase: N/A
Study type: Interventional

The number of people diagnosed with Type 2 diabetes (T2DM) is increasing rapidly and about 2.9 million people in the UK currently have diabetes. There is increasing evidence suggesting that prolonged sedentary time may actually increase the risk of diabetes and other chronic diseases. Importantly, adults can meet public health guidelines on physical activity (150 minutes of moderate activity per week), but if they still sit for prolonged periods, their metabolic health is compromised. Going from sitting to standing and carrying out light-intensity activities (such as casual walking) may reduce diabetes risk. However, no one has investigated the effect of standing and walking on markers of cardio-metabolic markers in individuals with a high risk of T2DM. Therefore, the aim is to find out whether reducing the amount of time people spend sitting and replacing it with standing and light intensity activity (walking) reduces glucose, insulin and triglyceride levels, therefore reducing the risk of diabetes.

NCT ID: NCT02066948 Completed - Clinical trials for Impaired Glucose Tolerance

Meal Patterning on Weight Loss With Changes to Body Comp, Muscle and Metabolic Health

S38
Start date: January 2014
Phase: N/A
Study type: Interventional

About two-thirds of adults in the United States are overweight or obese with likely adverse health consequences. A Moderate weight loss by dieting and exercise is recommended to improve health. We are interested to know whether eating dietary protein at different times of the day influences changes in body composition, muscle and indices of health. The purpose of this study is to examine the effects of within-day patterning of dietary protein intake (even vs. skewed) on energy-restriction and resistance training-induced changes in body composition, muscle size, appetite, and clinical health (including blood glucose and blood pressure).

NCT ID: NCT01993927 Completed - Clinical trials for Impaired Glucose Tolerance

Voglibose Tablets 0.2 / OD Tablets 0.2 Special Drug Use Surveillance "Long-term Use in Patients With Impaired Glucose Tolerance"

Start date: November 18, 2009
Phase:
Study type: Observational

The purpose of this study is to determine the safety and efficacy of long-term use of Voglibose (Basen) to prevent progression to type 2 diabetes mellitus in participants with impaired glucose tolerance in the routine clinical setting.