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Glucose Metabolism Disorders clinical trials

View clinical trials related to Glucose Metabolism Disorders.

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NCT ID: NCT00483769 Completed - Cystic Fibrosis Clinical Trials

One Year Glargine Treatment in CFRD Children and Adolescents

Start date: February 2006
Phase: Phase 4
Study type: Interventional

Glargine treatment can improve the clinical features in Cystic Fibrosis patients affected by glucose derangements

NCT ID: NCT00464529 Completed - Clinical trials for Glucose Metabolism Disorders

Accuracy and Safety of Real Time Continuous Glucose Monitoring Before, During and After Surgery

GluContinu
Start date: May 2007
Phase: N/A
Study type: Observational

The purpose of this study is to determine the safety and accuracy of the Real-Time Continuous Glucose monitoring System (RT-CGMS)in measuring glucose in patients scheduled for surgery; before, during and after surgery.

NCT ID: NCT00362323 Completed - Clinical trials for Dyslipidemia/Glucose Metabolism Disorder

Fenofibrate and Metformin Fixed Combination vs Metformin - FAME METFO

Start date: October 2006
Phase: Phase 3
Study type: Interventional

To demonstrate in patients with T2DM and dyslipidemia not appropriately controlled with a statin and receiving metformin, the superiority of a fixed combination of fenofibrate and metformin vs metformin alone on TG and additionally, if the superiority on TG is established, to demonstrate the superiority on HDL-C

NCT ID: NCT00361868 Terminated - Dyslipidemia Clinical Trials

Fenofibrate and Metformin Fixed Combination vs Rosiglitazone - FAME ROSI

Start date: June 2006
Phase: Phase 3
Study type: Interventional

Under conditions of first-line drug treatment in antidiabetic drug naïve/drug free patients with type 2 diabetes mellitus and dyslipidemia, to show that :- the efficacy of a fixed combination (FC) of fenofibrate and metformin on glycemic control is not inferior to that of rosiglitazone and the efficacy of FC of fenofibrate and metformin on triglyceride control is superior to that of rosiglitazone.

NCT ID: NCT00349128 Completed - Clinical trials for Dyslipidemia/Glucose Metabolism Disorder

Fenofibrate in Dyslipidemia and Metformin-Controlled Diabetes

Start date: January 2004
Phase: Phase 2/Phase 3
Study type: Interventional

The primary objective was to assess the effect of 3-month treatment of low and standard doses of fenofibrate in combination with stable dose of metformin on fasting triglycerides levels in patients with type 2 diabetes and dyslipidemia.

NCT ID: NCT00348725 Completed - Clinical trials for Dyslipidemia/Glucose Metabolism Disorder

Acceptability of a Fixed Combination of Fenofibrate and Metformin

Start date: April 2005
Phase: Phase 3
Study type: Interventional

The primary objective was to assess the acceptability of a 4-week treatment of 4 new fixed-dose combinations of fenofibrate and metformin, in patients with type 2 diabetes and dyslipidemia.

NCT ID: NCT00306826 Withdrawn - Clinical trials for Glucose Metabolism Disorders

Pioglitazone in Impaired Glucose Tolerance

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

In patients with impaired glucose tolerance (IGT), the researchers want to study the relative effects of pioglitazone, simvastatin, or the combination of both on: - intima media thickness (IMT) as an easily assessed marker of atherosclerosis - heart rate variability (HRV) as a marker of autonomic neuropathy - flow-mediated vasodilatation (FMD) of the brachial artery as a marker of endothelial function - vascular and metabolic lab parameters

NCT ID: NCT00221156 Completed - Clinical trials for Coronary Artery Disease

Acarbose and Secondary Prevention After Coronary Stenting

Start date: May 2005
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine whether the intervention for newly diagnosed abnormal glucose tolerance after coronary stenting will improve the long-term clinical outcome.

NCT ID: NCT00192621 Completed - HIV Infections Clinical Trials

Seronegatives and Metabolic Abnormalities Protocol 2 (SAMA002): Study to Compare the Effect of Kaletra and Combivir® in HIV-Negative Healthy Subjects

Start date: November 2004
Phase: Phase 4
Study type: Interventional

This is a randomised study of the effect of treatment with Combivir (zidovudine [AZT] and lamivudine [3TC]) and Kaletra (lopinavir [LPVr]), alone and in combination, on the development of abnormalities in lipid and glucose metabolism in HIV negative healthy subjects.

NCT ID: NCT00114855 Completed - Hyperlipidemia Clinical Trials

The Effect of Hypocol® on Lipids in Subjects With Mild Hypercholesterolemia and Mildly Elevated Blood Glucose

Start date: March 2005
Phase: N/A
Study type: Interventional

The purpose of this study is to determine to what degree Hypocol® (Red Yeast Rice) may lower low density lipoprotein (LDL)-cholesterol in a European population. The effect of Red Yeast Rice on fasting blood glucose and inflammatory markers will also be investigated.