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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: NCT00530881 Completed - Clinical trials for Type 2 Diabetes Mellitus

Randomized, Double-Blind, Placebo-Controlled, With PHX1149 in Patients With Type 2 Diabetes Mellitus

Start date: April 2006
Phase: Phase 2
Study type: Interventional

This will be a 4-week, multicenter, randomized, double-blind, parallel group, placebo-controlled, safety, tolerability, and efficacy study. Patients will be screened and be on one of three doses of PHX1149 (a new drug candidate for the treatment of Type 2 diabetes ) or placebo. The drug is a "DPP4 inhibitor"

NCT ID: NCT00527995 Completed - Clinical trials for Type 2 Diabetes Mellitus

Acute Effects of Sildenafil on Endothelial Function in People With Diabetes

Start date: August 2001
Phase: Phase 3
Study type: Interventional

This is a double-blind, placebo-controlled, cross-over trial using a single dose of 100 mg sildenafil or placebo in 40 subjects with T2DM without known cardiovascular disease. Effects on haemodynamic parameters, flow mediated dilatation (FMD) in brachial artery, cardiovascular autonomic function tests, and spontaneous baroreflex sensitivity (BRS) were investigated.

NCT ID: NCT00522470 Completed - Obesity Clinical Trials

Effects of Rosiglitazone on Serum Ghrelin and Peptide YY Levels

Start date: n/a
Phase: Phase 4
Study type: Interventional

We aimed to evaluate the effects of rosiglitazone on serum ghrelin and peptide yy levels in diabetic women.

NCT ID: NCT00522158 Completed - Clinical trials for Type 2 Diabetes Mellitus

Effects of Achieving Very Low LDL-Cholesterol After Treatment With Statins on Steroidogenesis and Cognition

Start date: n/a
Phase: Phase 4
Study type: Interventional

We aimed to compare the effect of achieving an LDL-cholesterol <70 vs an LDL-cholesterol <100 mg/dL with simvastatin or atorvastatin on adrenal and testicular steroidogenesis, and cognition in diabetic patients.

NCT ID: NCT00520065 Completed - Clinical trials for Type 2 Diabetes Mellitus

Comparison of Nutritional Products for People With Type 2 Diabetes

Start date: August 2007
Phase: Phase 2
Study type: Interventional

Part A: To compare the glucose and insulin responses of a standard tube feeding product to that of a diabetes-specific tube feeding product in individuals with type 2 diabetes. Part B: To compare the glucose response of a standard tube feeding product to that of a diabetes-specific tube feeding product when consumed by individuals with type 2 diabetes as a sole source of nutrition.

NCT ID: NCT00519727 Completed - Clinical trials for Type 2 Diabetes Mellitus

Safety Study of ISIS 325568 in Healthy Volunteers

Start date: August 2007
Phase: Phase 1
Study type: Interventional

The primary purpose of this trial is to assess the safety of ISIS 325568 when given at increasing single doses and to assess the safety of the same doses when given multiple times.

NCT ID: NCT00517283 Completed - Clinical trials for Type 2 Diabetes Mellitus

A Study by Scintigraphy to Evaluate the Effect of Exenatide on Gastric Emptying in Subjects With Type 2 Diabetes

Start date: January 2005
Phase: Phase 1
Study type: Interventional

As exenatide slows the rate at which materials leave the stomach, it is likely to alter the rate of intestinal absorption of oral drugs when administered within a certain timeframe relative to exenatide. In addition, the residence time within the stomach of other medication may be prolonged and data from this study will help assess the change in residence time in the presence of therapeutic doses of exenatide. This study will also evaluate the relationship between blood levels of exenatide and parameters measuring rate of stomach emptying.

NCT ID: NCT00516074 Completed - Clinical trials for Type 2 Diabetes Mellitus

A Study to Assess the Effect of Exenatide Treatment on Mean 24-Hour Heart Rate in Patients With Type 2 Diabetes

Start date: September 2007
Phase: Phase 3
Study type: Interventional

This study will explore the effect of exenatide (given twice a day) versus placebo (given twice a day) treatment on change in mean 24-hour heart rate over a 12 week period of drug exposure in patients with type 2 diabetes.

NCT ID: NCT00516048 Completed - Clinical trials for Type 2 Diabetes Mellitus

An Exploratory Study of the Effect of Treatment Interruption on Safety of Exenatide in Patients With Type 2 Diabetes

Start date: August 2007
Phase: Phase 3
Study type: Interventional

The primary purpose of this study is to assess the anti-exenatide-antibody response to exenatide re-exposure as measured by anti-exenatide antibodies and incidence of treatment-emergent allergy and hypersensitivity reactions following a period of treatment interruption, in patients previously exposed to exenatide.

NCT ID: NCT00515723 Completed - Schizophrenia Clinical Trials

Glucose and Lipid Metabolism on Antipsychotic Medication

Glulipid
Start date: September 2001
Phase: N/A
Study type: Interventional

This project aims to a) evaluate the effects of selected antipsychotic medications on insulin action in skeletal muscle (glucose disposal), liver (glucose production) and adipose tissue (whole-body lipolysis), b) evaluate the effects of selected antipsychotic medications on abdominal adipose tissue mass, total body fat and total fat-free mass, and c) explore the longitudinal effects of treatment with selected antipsychotics on glucose tolerance, lipid profiles, abdominal adipose tissue mass, total body fat and total fat-free mass. These hypotheses will be evaluated by measuring 1) whole-body glucose and lipid kinetics with the use of "gold-standard" stable isotope tracer methodology, 2) body composition using dual energy x-ray absorptiometry and magnetic resonance imaging, and 3) longitudinal changes in glucose tolerance and lipid profiles. The aims will be addressed in non-diabetic schizophrenia patients chronically treated with risperidone, olanzapine, clozapine, quetiapine, ziprasidone, or haloperidol, and untreated healthy controls. Re-evaluations will also be performed in patients who are randomized to switch from their current antipsychotic (from the above groups) to risperidone, olanzapine, quetiapine, or ziprasidone for 6 months. Relevant data is critically needed to target basic research, identify long-term cardiovascular consequences, and plan therapeutic interventions.