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Type 2 Diabetes Mellitus clinical trials

View clinical trials related to Type 2 Diabetes Mellitus.

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NCT ID: NCT01316094 Completed - Clinical trials for Type 2 Diabetes Mellitus

A Study to Assess Efficacy and Safety of ASP1941 in Diabetic Patients With Renal Impairment

Start date: January 18, 2011
Phase: Phase 3
Study type: Interventional

This study is to assess the effect of renal function on the efficacy and safety of ASP1941 in type 2 diabetic patients with mild to moderate renal impairment.

NCT ID: NCT01315977 Recruiting - Clinical trials for Type 2 Diabetes Mellitus

Dietary Antioxidants, Redox Tone and Health Promotion: an Orthomolecular Study of Interactions

Start date: February 2011
Phase: Phase 1/Phase 2
Study type: Interventional

Aging is associated with increased risk of various diseases, and much attention is given to the use of natural products (like herbs) and 'functional food', such as teas, for healthy aging. The body is continuously exposed to potentially damaging agents (known as free radicals). The imbalance between the amount of free radicals and that of antioxidants in the body is known as oxidative stress. It is known that Type 2 DM is a state of increased oxidative stress, which is thought to lead to many long term complications of Type 2 DM, such as heart disease, vision problems and kidney failure. Antioxidant therapy, including increased consumption of antioxidant rich foods and beverages such as green tea, has been suggested as possibly beneficial in lowering the risk of these complications. The purpose of this study is to examine the effects of regular intake of green tea on indices of oxidative stress and antioxidant defense within cells, plasma and urine so as to investigate if regular intake of green tea can be recommended for health promotion.

NCT ID: NCT01310452 Active, not recruiting - Clinical trials for Type 2 Diabetes Mellitus

Study on Liver Fat Content and Visceral Fat Mass in Overweight and Obese Type 2 Diabetes Patients After Treatment With Basal Insulin

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

Primary objective: To compare the change in liver fat content and visceral fat mass (cm2) assessed by MRS (Magnetic Resonance Spectroscopy) and MRI (Magnetic Resonance Image), after 26 weeks of treatment with insulin detemir once daily or insulin NPH once daily both with metformin in overweight and obese type 2 diabetic subjects. Secondary objectives: To compare the two treatments with respect to: 1. Efficacy: - MRI: abdominal subcutaneous fat mass(cm2), Calculated Visceral/Subcutaneous Adipose Tissue Ratio. - Change in HbA1c from baseline at 12 and 26 weeks of treatment. - Change in Fasting plasma glucose from baseline at 12 and 26 weeks of treatment. - Weight - Waist and hip circumference 2. Safety: - Incidence of hypoglycaemia in the 26 weeks of treatment with insulin detemir versus NPH - Lipid profile at the start and after 26 weeks of treatment - Incidence of Adverse events during the trial - Safety profile as measured by laboratory safety parameters (haematology, biochemistry) and physical examination/vital signs before and at the end of treatment

NCT ID: NCT01302145 Completed - Clinical trials for Type 2 Diabetes Mellitus

Drug to Drug Interaction Study With ASP1941 and Metformin

Start date: February 25, 2009
Phase: Phase 1
Study type: Interventional

A study to investigate the effect on safety, pharmacokinetics and pharmacodynamics when ASP1941 is administered as add-on therapy to metformin.

NCT ID: NCT01302028 Completed - Clinical trials for Type 2 Diabetes Mellitus

Renal Impairment Study With ASP1941

Start date: January 22, 2010
Phase: Phase 1
Study type: Interventional

A study to investigate if the pharmacokinetics of ASP1941 is different in Type 2 Diabetes Mellitus (T2DM) patients with different grades of renal failure compared with T2DM patients with normal renal function and healthy volunteers.

NCT ID: NCT01301833 Completed - Clinical trials for Type 2 Diabetes Mellitus

Long-term Safety Study of MP-513 in Patients With Type 2 Diabetes

Start date: February 2011
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the safety and efficacy of MP-513 (Teneligliptin) as monotherapy or in combination with oral antihyperglycaemic agent in patients with type 2 Diabetes for 52 weeks administration.

NCT ID: NCT01301196 Recruiting - Clinical trials for Type 2 Diabetes Mellitus

Reducing Sedentary Behaviour in Young Adults at Risk of Diabetes

STAND
Start date: October 2010
Phase: N/A
Study type: Interventional

Excessive periods of time spent sitting may be a risk factor for diabetes. Current lifestyles encourage large amounts of sitting (sedentary behaviour) through increasing car use, computers, and appealing screen-based home entertainment systems. Methods to help change such behaviours are now needed, particularly for those with a high risk of developing a chronic disease, such as diabetes. The investigators propose to decrease sedentary behaviour in a multi-ethnic group of young adults at risk of diabetes through an educational intervention (attending a workshop and having prompts). If successful, this could have significant public health benefits given the widespread nature of sedentary behaviour.

NCT ID: NCT01298882 Completed - Obesity Clinical Trials

Diacerein on Insulin Secretion in Diabetes

Start date: n/a
Phase: Phase 2
Study type: Interventional

Aim. To assess the effect of interleukin 1β (IL-1β) and tumor necrosis factor α (TNFα) inhibition with diacerein administration on insulin secretion and metabolic control of drug-naïve patients with type 2 diabetes mellitus (T2DM) and overweight or obesity. Hypothesis. Diacerein administration improves insulin secretion and metabolic control of drug-naïve patients with type 2 diabetes mellitus (T2DM) and overweight or obesity. Materials and methods. Design: Randomized, double-blind, placebo-controlled clinical trial. Population: 40 drug-naïve adult patients with T2DM and overweight or obesity. Measurements: A metabolic profile including IL-1β, TNFα, interleukin 6, and fasting insulin levels, as well as, hyperglycemic-hyperinsulinemic clamp technique; to assess the phases of insulin secretion and insulin sensitivity. Intervention for 2 mo: diacerein (50 mg once daily) for the first 15 days and twice daily for 45 additional days or placebo. Statistical analyses: Wilcoxon signed rank and Mann-Whitney U test.

NCT ID: NCT01298375 Recruiting - Healthy Clinical Trials

Metabolic Phenotyping in Humans

MetPhe
Start date: March 2011
Phase:
Study type: Observational

Type 2 diabetes (T2D) is a global burden disease affecting almost 200 million people and is expected to nearly double by 2030 (1). It is imperative that this disease is kept under control, and that we begin to reverse the direction of its incidence. We propose to start by identifying the physiological and molecular aspects of the problem in all spectrums of the disease (ie from insulin sensitive athletes to sedentary lean and obese individuals and further to overt type 2 diabetics), and focus our efforts on examining the differences and identifying the stages of progression for possible targets of future intervention. The proposed study "Metabolic Phenotyping" is novel in its target populations and innovative in its use of state-of-the-art techniques. We hypothesize that the in vivo differences in metabolic flexibility and mitochondrial function between endurance athletes and type 2 diabetics and their lean and obese controls are retained in vitro and will offer a new model in which to study the underlying mechanisms of the progression of T2D.

NCT ID: NCT01293669 Completed - Clinical trials for Type 2 Diabetes Mellitus

Glycemic Control, Safety and Tolerability of TC-6987 Monotherapy in Type 2 Diabetes Mellitus

Start date: January 2011
Phase: Phase 2
Study type: Interventional

TC-6987 is a selective nicotinic α-7 receptor ligand (open channel stabilizer) that has demonstrated potent anti-inflammatory/antioxidant properties in animal models. Following the oral administration of a 1mg/kg dose of TC-6987 to diabetic mice (db/db mouse) for 7 weeks, numerous metabolic improvements were observed. Specifically, plasma glucose and triglyceride concentrations declined by approximately 30%; Hb1Ac was reduced by nearly 50%; and TNF-α declined more than 60% relative to control db/db mice Therefore, it appears that TC-6987 could prove beneficial in reducing elevated glucose concentrations in diabetic patients as well as in ameliorating organ damage associated with inflammation, oxidative stress and hyperglycemia.