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Glucose Intolerance clinical trials

View clinical trials related to Glucose Intolerance.

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NCT ID: NCT02621008 Recruiting - Hypertension Clinical Trials

Mobile Phone-based Intervention for Promoting Healthy Habits and Weight Loss

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

A self administered 16 weeks plus follow up study to explore the efficacy of mobile phone driven apps for stress reduction coupled with guidance for healthy living among obese and overweight populations. The Study primary end points are weight of the participants, as well as glucose measurements (for subject with diabetes) and blood pressure (of subjects with hypertension).

NCT ID: NCT02609243 Recruiting - Obesity Clinical Trials

Diabetes Nutrition Algorithm - Prediabetes

DiNA-P
Start date: July 2013
Phase: N/A
Study type: Interventional

Prediabetes, defined by either impaired fasting glucose and/or impaired glucose tolerance, is a known high-risk condition predisposing to future diabetes mellitus type 2. Strategies to prevent progression from prediabetes to diabetes have been widely studied, however, without striking long-term effects of any kind of intervention (pharmacological, behavioral...). The investigators therefore investigate certain nutritional approaches concerning nutrient content and favorable food components, targeting metabolic improvement.

NCT ID: NCT02605148 Active, not recruiting - Type 1 Diabetes Clinical Trials

TEFA Family Prevention: Glutenfree Diet to Preserve Beta-cell Function

TEFA
Start date: December 2015
Phase: N/A
Study type: Interventional

To evaluate the effect of Gluten Free Diet (GFD) on beta-cell function and glucose metabolism in subjects with one or several islet autoantibodies without and with dysglycemia at baseline. Additionally, all subjects will be given treatment with Vitamin D, omega fatty acids and probiotics. Subjects will be randomized to GFD or normal diet during 18 months. Beta cell function will be evaluated at baseline, and during follow-up by glucose tolerance tests.

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: NCT02569229 Completed - Cystic Fibrosis Clinical Trials

Glucose Tolerance in Children With Cystic Fibrosis

GluTolCF
Start date: June 2015
Phase:
Study type: Observational

The aim is to describe the association of glucose tolerance measured with three different tools (continuous glucose measurement system - CGMS, oral glucose tolerance testing - OGTT and optional intravenous glucose tolerance testing -IVGTT) with parameters out of lung function and anthropometric parameters in patients with cystic fibrosis.

NCT ID: NCT02565979 Completed - Pre-diabetes Clinical Trials

Long-term Resveratrol and Metabolism

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

The main objective of the study is to investigate if 6 months resveratrol supplementation can improve glucose tolerance in overweight/obese individuals. As secondary objectives we want to investigate whether resting energy metabolism, intra-hepatic lipid content, physical performance, body composition and quality of life change by 6 months resveratrol supplementation in these individuals.

NCT ID: NCT02559479 Recruiting - Obesity Clinical Trials

A Study to Assess the Effect of a Normal vs. High Protein Diets in Carbohydrates Metabolism in Obese Subjects With Diabetes or Prediabetes

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

The objective of the study is to assess the effect of low-calorie diets with normal (18%) vs. high (35%) protein (mainly coming from animal source) composition on body weight and carbohydrates metabolism in overweight and obese subjects with pre-diabetes or diabetes. A dietary intervention is carried out during 6 months in 100 subjects who are individually randomized to an energy-restricted diet with two types of macronutrients composition: 1) 35% protein, 30% fat and 35% carbohydrates and 2) 18% protein, 30% fat and 52% carbohydrates. Around 80% of total protein in diet comes from animal source (of whom around 40% from lean red meat). Subjects are provided with weekly menus and different recipes to use them as part of the diet. Monitoring visits with the nutritionist will be performed every 15 days. At the beginning of the study, after 3 and 6 months, the following parameters are determined: anthropometric (weight, waist circumference, body mass index and body composition), blood pressure, dietary (72-hours dietary registry) and exercise and biochemical analysis (total cholesterol, triglycerides, HDL cholesterol, LDL cholesterol, apolipoproteins A1 and B, iron, transferring, ferritin, uric acid, glucose, HbA1c, insulin, adiponectin and resistin). Urine samples are also collected to assess microalbuminuria and ureic nitrogen.

NCT ID: NCT02552355 Completed - Physical Activity Clinical Trials

Milk Protein Feeding After Aerobic Exercise in Older Adults With Pre-diabetes Taking the Biguanide Metformin

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

The investigators propose that post-exercise milk protein feeding will enhance the mitochondrial protein synthesis (biogenesis) response to an exercise-training program. In addition, the investigators propose that this stimulatory effect of protein feeding will overcome the potential blunting effect of metformin on exercise responses. The investigators will investigate these outcomes over a 12-week exercise-training program in older adults with pre-diabetes with or without metformin treatment.

NCT ID: NCT02520258 Completed - Clinical trials for Glucose Metabolism Disorder

Study of the Reversibility of Glucose Intolerance Caused by Chronic Aspartame Consumption

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

Experiments have shown that some artificial sweeteners like those in diet soda can cause changes in how the body responds to and uses sugar. These changes increase the chance of obesity, type 2 diabetes, and other metabolic diseases. In this study, the investigators plan to see if the most common artificial sweetener, aspartame (brand name Equal, NutraSweet), causes these changes. The investigators believe that if metabolic changes are observed in a person who consumes aspartame, then removing all aspartame from the diet might lead to a reversal of the changes and a normalization of test results.This would impact sweetener additives in our foods and thus decrease the incidence of obesity, diabetes, and the metabolic syndrome.

NCT ID: NCT02519309 Completed - Clinical trials for Diabetes Mellitus, Type 2

Dietary Intervention in Type-2 Diabetes and Pre-Diabetes

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

The primary purpose of this research is to demonstrate the therapeutic effects of implementing a well-formulated low carbohydrate lifestyle program over 2 years in patients with type 2 diabetes, pre-diabetes, and metabolic syndrome.