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Diabetes Mellitus, Type 2 clinical trials

View clinical trials related to Diabetes Mellitus, Type 2.

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NCT ID: NCT00485758 Completed - Clinical trials for Diabetes Mellitus Type 2

Extended Niacin/Laropiprant in Patients With Type 2 Diabetes (0524A-069)

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

A study to assess the efficacy and tolerability of ER (Extended Release) niacin/laropiprant versus placebo in Type 2 Diabetes Mellitus patients.

NCT ID: NCT00485056 Completed - Diabetes Clinical Trials

Pioglitazone on Cardiac Function and Large Arteries (PICCOLA Study)

PICCOLA
Start date: April 2008
Phase: Phase 4
Study type: Interventional

This study aims to use a novel, sensitive, non-invasive scanning technique to investigate the effects of insulin-sensitizing agent pioglitazone, on heart and artery function.

NCT ID: NCT00482976 Completed - Diabetes Mellitus Clinical Trials

Effect of LY333531 on Vascular and Neural Functions

Start date: December 2003
Phase: Phase 2
Study type: Interventional

To determine if protein kinase C beta plays a significant role in vascular endothelial dysfunction, small fiber neural dysfunction, and oxidative stress associated with diabetes mellitus.

NCT ID: NCT00482079 Completed - Clinical trials for Diabetes Mellitus, Type II

A Study of MK0431 in Patients With Type 2 Diabetes (0431-010)

Start date: May 13, 2003
Phase: Phase 2
Study type: Interventional

A dose-ranging study of MK0431 in patients with type 2 diabetes who have inadequate control of their blood sugar.

NCT ID: NCT00481286 Completed - Hypertension Clinical Trials

Improving Outcomes Using Collaborative Group Clinics to Empower Older Patients

EPIC
Start date: April 2007
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if group clinics help older veterans change behaviors with the goal of improving diabetes outcomes.

NCT ID: NCT00478322 Completed - Obesity Clinical Trials

Pharmacodynamic Study of the Effect of INCB013739 on Insulin Sensitivity in Obese, Type 2 Diabetic Subjects

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

Purpose: A 28-day US study in patients with type 2 diabetes mellitus to assess the safety and tolerability as well as the effects of treatment with an investigational drug.

NCT ID: NCT00476931 Completed - Clinical trials for Diabetes Mellitus, Type 2

Clinical Trial of SB-509 in Subjects With Diabetic Neuropathy

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

The purpose of the study is to study the clinical effects of the investigational drug, SB-509 versus placebo in patients with diabetic neuropathy.

NCT ID: NCT00476658 Completed - Obesity Clinical Trials

Macrophage Infiltration in Human Adipose Tissue

Start date: January 2007
Phase: N/A
Study type: Observational

Quantification of macrophage infiltration and characterization of macrophage phenotype in adipose tissue of 60 obese subjects and 20 non obese subjects

NCT ID: NCT00476437 Completed - Clinical trials for Diabetes Mellitus, Type 2

Safety and Effect of Biphasic Insulin Aspart 50 in Patients With Type 2 Diabetes Mellitus.

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

This trial is conducted in Japan. The purpose of this trial is to investigate the safety and the effect of biphasic insulin aspart 50 compared to biphasic human insulin 50 in patients with type 2 diabetes mellitus.

NCT ID: NCT00476281 Completed - Diabetes Clinical Trials

Nutritional, Metabolic and Respiratory Status in Cystic Fibrosis

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

Diabetes is a important complication of cystic fibrosis (CF). The improved life expectancy of patients with cystic fibrosis, as a result of advances in medical therapy, has resulted in an increasing prevalence of cystic fibrosis-related diabetes (CFRD). CFRD is associated with accelerated pulmonary decline and increased mortality. Pulmonary effects are seen some years before the diagnosis of CFRD implying that impaired glucose tolerance may be very early detrimental. Insulin treatment is clearly indicated in patients with CFRD to control symptoms and reduce complications. However, at the state of impaired glucose tolerance or fasting hyperglycaemia, current screening methods are not suitable for the early management of hyperglycaemia.The recent introduction of the continuous glucose monitoring system (CGMS), which provides a continuous glucose profile, has revealed to be clinically relevant in the investigation of glucose excursions over a long period. This device, widely use in diabetic non cystic fibrosis patients, has been validated in non diabetic cystic fibrosis subjects. Previous studies of continuous glucose monitoring have been realized in CF patients with normal glucose tolerance and diabetes and compared with non CF controlThe aim of our study is to evaluate the glucose profile with continuous glucose monitoring the nutritional and respiratory status in cystic fibrosis subjects, according to their glucose tolerance.