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Glucose Metabolism Disorders clinical trials

View clinical trials related to Glucose Metabolism Disorders.

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NCT ID: NCT03181191 Completed - Clinical trials for Glucose Metabolism Disorders

The Anatomical Location, Cellular Origin and Molecular Basis of Gut-derived Glucagon Secretion

Start date: April 27, 2017
Phase: N/A
Study type: Interventional

Delineation of the anatomical location, cellular origin and molecular basis of gut-derived glucagon secretion

NCT ID: NCT03162991 Completed - Physical Activity Clinical Trials

Aerobic Treadmill Exercise And Metabolism

The A-TEAM
Start date: November 13, 2017
Phase: N/A
Study type: Interventional

Overview- In this study, overweight or obese, sedentary participants (age=35-55 years, n=20) will be randomized to a 12-week control period or an aerobic exercise intervention. Those randomized into the control group will then complete the exercise intervention subsequently. The planned energy expenditure per week of exercise will be 10-12 kilocalories per kilogram of body weight per week. Participants will complete three non-consecutive exercise sessions per week. Body weight, resting metabolic rate via indirect calorimetry, peak oxygen consumption (VO2peak) through graded exercise testing, fasting blood samples, CGM, sleep and dietary habits via self-report, and physical activity monitoring will be completed at prior to and following the aerobic exercise intervention.

NCT ID: NCT03151239 Completed - Clinical trials for Glucose Metabolism Disorders

Effect of "Nicotinamide Mononucleotide" (NMN) on Cardiometabolic Function

NMN
Start date: July 1, 2017
Phase: N/A
Study type: Interventional

The purpose of the study is to understand the effect of the dietary supplement "Nicotinamide mononucleotide" on metabolic health in people.

NCT ID: NCT03133741 Completed - Clinical trials for Glucose Metabolism Disorders

Inhibition of the Endogenous GIP Response With a GIP Receptor Antagonist

GA-3
Start date: March 1, 2017
Phase: N/A
Study type: Interventional

Delinieation of GIP's effects during an oral glucose tolerance test (OGTT) in humans using GIP receptor antagonisation.

NCT ID: NCT03090074 Recruiting - Clinical trials for Glucose Metabolism Disorders

Moderate or Extensive Carbohydrate Reduction in Risk Patients

LOWinCHIP
Start date: March 20, 2017
Phase: N/A
Study type: Interventional

Risk-patients for diabetes or patients that are diagnosed with this condition but who are not treated with insulin are randomized two times, according to diet and according to the type of support: Randomization with regard to carbohydrate restriction (25-30 E% or < 10E%). Randomization with regard to type of psychological support. Either according to Acceptance and Commitment Therapy or to traditional cognitive behavioral therapy. Both kinds of psychological support is given as group therapy. Two-hundred patients are recruited and each patient is followed for two years.

NCT ID: NCT03067428 Completed - Clinical trials for Endothelial Dysfunction

Effects of Fructose Restriction on Liver Steatosis

FRUITLESS
Start date: January 31, 2017
Phase: N/A
Study type: Interventional

Nonalcoholic fatty liver disease (NAFLD) is an emerging health problem as it can lead to end stage liver failure and cardiovascular complications. Diet play an important role in the development of NAFLD. Many studies have addressed the effects of added fructose on NAFLD. To date, little attention has been paid to the effects of a diet devoid of fructose. Therefore, the investigators aim to study the effects of fructose restriction on hepatic fat accumulation and vascular function using a double-blind randomized placebo-controlled design.

NCT ID: NCT03059550 Recruiting - Diabetes Clinical Trials

Screening for Glucose Metabolism Disorders in Cardiac Rehabilitation

REHABDIAB
Start date: March 1, 2013
Phase:
Study type: Observational

Because prevalence of glucose metabolism disorders is high in patients with coronary disease, the Oral Glucose Tolerance Test (OGTT) is recommended in all patients without diabetes after an acute coronary syndrome (ACS). However, there are some concerns about its performance in clinical practice. The aim of our study was to evaluate, after an acute coronary syndrome (ACS), the feasibility and efficacy of the OGTT in a cardiac rehabilitation (CR) center in comparison with its real application in the whole French population.

NCT ID: NCT03056677 Completed - Clinical trials for Metabolism Disorder, Glucose

Modified Whey Protein and Effect on Post Meal Glucose Levels Study

MWPS
Start date: August 2016
Phase: N/A
Study type: Interventional

After meals, the level of glucose rises in the circulation. In some individuals who are overweight and older, blood glucose can rise to levels which can damage tissues and cause health problems. Usually the hormone insulin, released from the pancreas, effectively lowers blood glucose. However, in overweight and older people insulin is less effective. Certain foods can lower the rise in blood glucose, particularly proteins. This works by increasing the release of a hormone from the gut called Glucagon-Like Peptide 1 (GLP-1), which in turn increases the release of insulin. A Component of milk left over after cheese making, termed Whey protein, is particularly good at releasing GLP-1. Whey protein is used as a food additive and taken as a supplement to help build muscle. Whey protein is a mixture of proteins which the investigators have modified to be more effective at lowering blood glucose. Using laboratory tests the investigators identified a protein present in Whey that does not increase levels of GLP-1 and removed it. It's removal raises the levels of other proteins which are more effective. In this study, the investigators would like to test the effectiveness of the "modified" whey protein. To do this, 30 older, overweight volunteers will be recruited and given the modified whey protein, a normal whey protein or a mixture of amino acids and then a breakfast meal to raise their blood glucose levels. These drinks will be given in a randomised sequence 1 week apart. On each visit, blood samples to measure blood glucose and related hormone levels will be taken. As GLP-1 can also have an effect on appetite, the investigators will measure the effect of the modified whey protein on subsequent appetite in the volunteers by asking them how hungry they feel.

NCT ID: NCT03041363 Completed - Epilepsy Clinical Trials

Treatment Development of Triheptanoin (G1D)

Start date: March 29, 2017
Phase: Phase 1
Study type: Interventional

To determine the maximum tolerated dose (MTD), as a percentage of calories consumed, of triheptanoin (C7 oil; C7) in a pediatric and adult patient population genetically diagnosed with glucose transporter type 1 deficiency disorder (G1D).

NCT ID: NCT03013296 Completed - Clinical trials for Glucose Metabolism Disorders

Delinieation of GIP's Effects During a Meal in Humans Using GIP Receptor Antagonisation (GA-4)

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

Delinieation of GIP's effects during a meal in humans using GIP receptor antagonisation.