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| Sponsor: | University of Science Malaysia |
|---|---|
| Collaborator: |
Ministry of Health, Malaysia |
| Information provided by: | University of Science Malaysia |
| ClinicalTrials.gov Identifier: | NCT00489229 |
Purpose
The aim is to examine whether pharmacological interventions with thiazolidinedione and angiotensin converting enzyme (ACE) inhibitors can reverse pre-clinical vasculopathy in newly diagnosed diabetic and IGT individuals.
| Condition | Intervention | Phase |
|---|---|---|
|
Diabetes Impaired Glucose Tolerance |
Drug: Rosiglitazone Drug: Ramipril |
Phase III |
| Study Type: | Interventional |
| Study Design: | Treatment, Randomized, Double-Blind, Placebo Control, Factorial Assignment, Efficacy Study |
| Official Title: | Studies on Diabetic and Pre Diabetic Vascular Disease and the Effect of Selected Therapeutic Modalities on Associated Vasculopathy |
| Enrollment: | 66 |
| Study Start Date: | October 2002 |
| Study Completion Date: | December 2005 |
The burden of diabetic vasculopathy on the global population is enormous and ever growing. Besides the well-known microvascular complications in type 2 diabetes (T2DM), there is a growing epidemic of macrovascular complications. People with T2DM have a higher risk of death from cardiovascular (CV) diseases than persons without diabetes. Like diabetes, impaired glucose tolerance (IGT) individuals also have associated risk of developing macrovascular complications. This calls for an early detection and intervention in patients with T2DM as well as IGT, not only to delay progression of IGT to T2DM but also to treat early macrovascular diseases in both groups. The traditional therapeutic approaches of T2DM emphasise on glycaemic control, which limits microvascular diseases but lacks an established benefit in macrovascular diseases. Type 2 diabetes is a metabolic disorder characterised by dyslipidaemia, hypertension, and hypercoagulability in addition to hyperglycaemia and hyperinsulinaemia. Each of these abnormalities plays an important role in diabetic vasculopathy and provides targets for therapy. Understanding the mechanisms of diabetic vasculopathy and instituting therapy guided by emerging evidences would improve outcomes in patients with T2DM and IGT.
In recent years, special attention has been devoted to both thiazolidinediones (TZDs) and angiotensin converting enzyme (ACE) inhibitors when TRIPOD study demonstrated that troglitazone may reduce the rate of progression to diabetes in women diagnosed with gestational diabetes and HOPE Study showed that ramipril may delay the onset of diabetes. The TZDs are novel insulin-sensitising antidiabetic agents, which also have vasculoprotective properties. Rosiglitazone, one of the members of TZD family, improves insulin sensitivity and may have a beta cell cytoprotective effect. The ACE inhibitors reduce both microvascular and macrovascular complications in diabetes and appear to improve insulin sensitivity and glucose metabolism. Ramipril, an ACE inhibitor, has direct effects on the renin-angiotensin-kallikrein system and may play an important role in the prevention of diabetes through effects on beta cell and by vascular and metabolic effects on muscle that may amplify the effects of insulin. Previous studies showed that newly diagnosed untreated T2DM/IGT and hypertensive Malay patients had early manifestations of preclinical vasculopathy and potentially increased risk for development of macrovascular diseases. The aim of this study is to investigate whether pharmacological interventions with rosiglitazone and ramipril can reverse pre-clinical vasculopathy in newly diagnosed untreated T2DM and IGT patients.
Eligibility| Ages Eligible for Study: | 30 Years to 65 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Contacts and Locations| Malaysia, Kelantan | |
| School of Medical Sciences, University Sains Malaysai | |
| Kota Bharu, Kelantan, Malaysia, 16150 | |
| Study Director: | Abdul Rashid A Rahman, MRCP, PhD | Universiti Sains Malaysia |
More Information
| Study ID Numbers: | ID: 305/PPSP/6112215 |
| Study First Received: | June 20, 2007 |
| Last Updated: | July 15, 2009 |
| ClinicalTrials.gov Identifier: | NCT00489229 History of Changes |
| Health Authority: | Malaysia: Ministry of Health |
|
Rosiglitazone Ramipril Impaired glucose tolerance Arterial stiffness Diabetic vasculopathy |
|
Metabolic Diseases Molecular Mechanisms of Pharmacological Action Physiological Effects of Drugs Glucose Intolerance Diabetes Mellitus Vascular Diseases Endocrine System Diseases Enzyme Inhibitors Cardiovascular Agents Antihypertensive Agents Pharmacologic Actions |
Ramipril Protease Inhibitors Diabetic Angiopathies Hypoglycemic Agents Hyperglycemia Therapeutic Uses Angiotensin-Converting Enzyme Inhibitors Cardiovascular Diseases Glucose Metabolism Disorders Rosiglitazone Diabetes Complications |