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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: NCT01847092 Completed - Clinical trials for Type 2 Diabetes Mellitus

A Study in CKD Patients With Type 2 Diabetes Mellitus and Albuminuria

Start date: May 2013
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine if the study drug is safe, tolerable and active in reducing albuminuria in patients with Chronic Kidney Disease with Type 2 Diabetes.

NCT ID: NCT01844050 Completed - Clinical trials for Type 2 Diabetes Mellitus

Traditional Chinese Medicine in Individualized Treatment of Patients With Diabetes Symptoms

Start date: September 2008
Phase: N/A
Study type: Interventional

Based on the Individualized treatment of diabetes symptoms to evaluate the method of syndrome differentiation treatment of Traditional Chinese medicine.

NCT ID: NCT01843881 Completed - Clinical trials for Type 2 Diabetes Mellitus

The Contribution of Incretin Hormones to Post-prandial Glucose Metabolism After Roux-en-Y Gastric Bypass

Start date: March 2012
Phase: Phase 0
Study type: Interventional

The study is being undertaken to understand how the Roux-en-Y Gastric Bypass procedure can affect insulin secretion after meals. The hypothesis of this study is the Disposition Index is decreased in subjects who had previously undergone Roux-en-Y Gastric Bypass by glucagon-like peptide-1 (GLP-1) receptor blockade.

NCT ID: NCT01843855 Completed - Clinical trials for Type 2 Diabetes Mellitus

The Contribution of Incretin Hormones to the Amelioration of Glucose Metabolism After Roux-en-Y Gastric Bypass

Start date: June 2011
Phase: Phase 0
Study type: Interventional

The study is being undertaken to understand how a gastric bypass can affect a subject's diabetes even prior to their losing significant amounts of weight. The hypothesis of this study is that increased glucagon-like peptide-1 (GLP-1) secretion explains the amelioration in insulin secretion after Roux-en-Y Gastric Bypass (RYGB) surgery.

NCT ID: NCT01843127 Completed - Clinical trials for Type 2 Diabetes Mellitus

A Study to Evaluate the Effect of Ranolazine on Postprandial Glucagon in Subjects With Type 2 Diabetes.

Start date: April 2013
Phase: Phase 1
Study type: Interventional

To explore the mechanism of action of ranolazine as a potential treatment for type 2 diabetes mellitus (T2DM).

NCT ID: NCT01832935 Completed - Clinical trials for Type 2 Diabetes Mellitus

Cost Effectiveness of Glargine Insulin Versus NPH Insulin

Start date: July 2011
Phase: Phase 4
Study type: Interventional

Glycemic control is fundamental in the management of diabetes mellitus .If lifestyle intervention and full tolerated doses of one or two oral glucose lowering drugs (OGLDs) fail to achieve or sustain glycemic goals, insulin should be initiated. New insulin analogs are generated to improve glycemic control .New insulin analogs are generated to improve glycemic control,However, the cost of these analogs is a major problem .The aim of this piggy back evaluation was to assess the effect of Glargine insuline versus NPH plus regular human insulin on metabolic control as well as its cost-effectiveness in people with type 2 diabetes in the Iranian setting.

NCT ID: NCT01832311 Completed - Clinical trials for Type 2 Diabetes Mellitus

Protein Profile of Immunoregulatory Factors in Diabetic Cataract

Start date: January 2009
Phase: Phase 4
Study type: Interventional

The purpose of this study is to compare the levels of several immunoregulatory factors in serums and aqueous humor of type II diabetes cataract patients with those in senile non-diabetic cataract patients since disturbed cytokine and growth factor microenvironment in diabetic eye may contribute to an increased frequency of intraoperative and postoperative intraocular lens surgery complications.

NCT ID: NCT01828931 Completed - Schizophrenia Clinical Trials

Lifestyle Intervention for Diabetes and Weight Management in Psychosis

Healthy_LIFE
Start date: December 2012
Phase: N/A
Study type: Interventional

The rate of type-2 diabetes mellitus (T2DM) is at least 2-3 times higher in persons with psychotic illnesses than in the general population. Life expectancy of individuals with psychosis is also 20-25 years less than the general population, primarily due to premature onset of cardiovascular disease (CVD). Despite the high risk for T2DM and CVD, psychotic illness has been an exclusion criterion in all large-scale studies of diabetes prevention and management. We propose a 3-year randomized controlled trial examining the effectiveness of a lifestyle intervention (LI) aimed at reducing caloric intake and increasing physical activity in overweight or obese individuals (N=150) suffering from both a psychotic illness and T2DM. Weight and glycemic control will be the primary outcome variables. It is hypothesized that a significant weight reduction and improvement in glycemic control will be found in those who receive the LI relative to those who do not.

NCT ID: NCT01826162 Completed - Obesity Clinical Trials

Short Chain Fatty Acid Metabolism and Energy Metabolism

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

Gut microbiota is being increasingly recognized as an important factor in fat distribution, insulin sensitivity and glucose and lipid metabolism. Accordingly, the intestinal microbiota could play an important role in the development of obesity and type 2 diabetes mellitus. The role of gut-derived short-chain fatty acids (SCFA), the formation of which is enhanced by microbial fermentation of fibre, is still controversial. At the present time, our understanding of the effects of SCFA on human metabolism (in gut or systemically) is still limited. The investigators hypothesize that the differential availability of SCFA impacts human metabolism differently. In this placebo controlled, double-blind, randomized crossover pilot study the investigators will validate in overweight/obese healthy male volunteers whether rectal administration of SCFA is a good model for studying the acute metabolic effects of SCFA. For this, it will be investigated if site of administration (in distal or proximal colon) of SCFA differentially affects parameters of substrate and energy metabolism and to test the duration of short-term effects of SCFA administration.

NCT ID: NCT01823510 Completed - Clinical trials for Coronary Artery Disease

Ticagrelor Versus Clopidogrel in Type 2 Diabetic Patients

Start date: July 2013
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether treatment with ticagrelor + aspirin is more effective than treatment with clopidogrel + aspirin in patients with type-2 diabetes. Both treatments will be given (separately) to all subjects as a one-time loading dose (i.e. higher than a normal daily dose), followed by daily dose for the next 5 to 7 days. Effectiveness of treatment will be measured with specialized blood tests before the loading dose, at two time-points after the loading dose, and once after the last daily dose.