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Type 2 Diabetes clinical trials

View clinical trials related to Type 2 Diabetes.

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NCT ID: NCT01771042 Not yet recruiting - Obesity Clinical Trials

The Effects of Weight Loss on Neuroadrenergic Function

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

Elevated subconscious nervous system activity is a characteristic of the obese state and contributes importantly to the risk of heart disease and diabetes. This project will compare sympathetic nervous system activity and function in a group of obese persons with differing levels of sugar tolerance (normal, impaired and type 2 diabetic). Inter-relationships with insulin action, blood pressure, heart and kidney function will be determined before and after a 4-month weight loss and 3-month weight loss maintenance program. It is hypothesized that the transition from normal sugar tolerance to impaired sugar tolerance to type 2 diabetes will be accompanied by escalating sympathetic nervous system dysfunction. Furthermore, that weight loss will favorably improve sympathetic function, with greatest benefits occurring in those subjects who are insulin resistant with high blood insulin concentration.

NCT ID: NCT01768559 Completed - Type 2 Diabetes Clinical Trials

Efficacy and Safety of Lixisenatide Versus Insulin Glulisine on Top of Insulin Glargine With or Without Metformin in Type 2 Diabetic Patients

GetGoal Duo-2
Start date: January 2013
Phase: Phase 3
Study type: Interventional

Primary Objective: - To compare lixisenatide versus insulin glulisine in terms of HbA1c reduction and body weight change at week 26 in type 2 diabetic patients not adequately controlled on insulin glargine ± metformin. Secondary Objectives: - To compare the treatments/regimens on: - The percentage of patients reaching the target of HbA1c <7% or ≤6.5% - Body weight - Self-Monitored Glucose profiles - Fasting Plasma Glucose (FPG) - Post-prandial plasma glucose /glucose excursions during a standardized meal test (subset of patients) - Daily doses of insulins - Safety and tolerability

NCT ID: NCT01768208 Active, not recruiting - Type 2 Diabetes Clinical Trials

Metabolomic Variations in the Saxagliptin-Treated Type 2 Diabetes Mellitus Patients

Start date: October 2012
Phase: Phase 4
Study type: Interventional

This study is an open-label, cohort study to evaluate the potential mechanisms of Saxagliptin in the treatment of patients with type 2 diabetes (T2DM) using a comprehensive metabolomic method, in combination with fingerprint analysis and target analysis. It is a sub-study of STUDY: D168L00008.

NCT ID: NCT01766752 Completed - Type 2 Diabetes Clinical Trials

Performance of a Tablet Based Workflow and Decision Support System With Incorporated Software Algorithm Used for Glycaemic Management

Start date: November 2012
Phase: Phase 3
Study type: Interventional

Objective: To investigate the performance (safety) of the GlucoTab system for glycaemic management in non-critically ill patients with type 2 diabetes at the general ward

NCT ID: NCT01763346 Completed - Obesity Clinical Trials

Beta Cell Restoration Through Fat Mitigation

BetaFat
Start date: June 2013
Phase: N/A
Study type: Interventional

Weight loss achieved through gastric banding will be superior to treatment with metformin in preserving or restoring pancreatic beta cell function in people with prediabetes or mild type 2 diabetes.

NCT ID: NCT01758471 Recruiting - Type 2 Diabetes Clinical Trials

Efficacy of Acarbose on Intestinal Microbiome and Incretins of Type 2 Diabetes

Start date: December 2012
Phase: Phase 4
Study type: Interventional

This study is aimed to investigate the effect of acarbose on intestinal microbiome and incretins, therefore to explore the new pathways or new targets to treat type 2 diabetes.

NCT ID: NCT01757587 Completed - Type 2 Diabetes Clinical Trials

Galvus (Vildagliptin) vs Placebo in Combination With Metformin and Insulin

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

The main objective is to show that the addition of Galvus versus placebo in patients with type 2 diabetes treated with metformin (at the maximum tolerated dose) and basal insulin properly titrated, allows a greater proportion of patients achieving an HbA1c below 7%. The primary efficacy endpoint was the percentage of patients responding to treatment (HbA1c less than 7%) after 3 months of treatment with Galvus or placebo

NCT ID: NCT01755572 Completed - Type 2 Diabetes Clinical Trials

Blood Pressure Outcomes With Liraglutide Therapy

BOLT
Start date: January 2013
Phase: Phase 4
Study type: Interventional

Purpose: The purpose of this study is to further study the mechanism by which liraglutide, a relatively new anti-hyperglycemic medication, might lower blood pressure in patients with Type 2 diabetes and high blood pressure.

NCT ID: NCT01755468 Completed - Type 2 Diabetes Clinical Trials

Early Intermittent Intensive Insulin Therapy as an Effective Treatment of Type 2 Diabetes (RESET-IT Pilot Study)

Start date: April 2013
Phase: Phase 3
Study type: Interventional

Type 2 diabetes mellitus is a chronic metabolic disorder characterized by progressive deterioration in the function of the pancreatic beta-cells, which are the cells that produce and secrete insulin (the hormone primarily responsible for the handling of glucose in the body). The investigators propose a pilot randomized controlled trial to determine whether intermittent intensive insulin therapy is an effective therapeutic strategy that can preserve pancreatic beta-cell function and maintain glycemic control early in the course of type 2 diabetes.

NCT ID: NCT01754792 Completed - Healthy Clinical Trials

Effects of Pinitol on Hidrocarbonated Metabolism Parameters in Diabetic, Impaired and Normal Fasting Glucose Subjects

Start date: January 2012
Phase: N/A
Study type: Interventional

The purpose of this study was to assess whether pinitol improves hidrocarbonated metabolism parameters, and evaluate its effect on oxidative stress and endothelial function in diabetic, impaired and normal fasting glucose subjects. This was a 3-month randomised, controlled-placebo, parallel trial with a three-arm design. Patients were divided into three groups: diabetic (n=40), impaired fasting glucose (n=40) or normal fasting glucose subjects (n=40), receiving 4 g/day of pinitol/placebo.