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| Sponsor: | Boehringer Ingelheim Pharmaceuticals |
|---|---|
| Information provided by: | Boehringer Ingelheim Pharmaceuticals |
| ClinicalTrials.gov Identifier: | NCT00274118 |
Purpose
To compare the renal consequences of two different approaches to blocking the renin angiotensin system in subjects with hypertension and concurrent Type II diabetes mellitus and diabetic nephropathy.
| Condition | Intervention | Phase |
|---|---|---|
|
Hypertension Diabetes Mellitus, Type 2 |
Drug: telmisartan Drug: enalapril |
Phase III |
| Study Type: | Interventional |
| Study Design: | Prevention, Randomized, Double-Blind, Active Control, Parallel Assignment, Efficacy Study |
| Official Title: | A Randomised ,Double-blind ,Parallel-group Comparison of the Renal and Antihypertensive Effects of Telmisartan and Enalapril in Subjects With Mild to Moderate Hypertension and Concurrent Type II Diabetes Mellitus and Diabetic Nephropathy. |
| Estimated Enrollment: | 272 |
| Study Start Date: | July 1997 |
| Estimated Study Completion Date: | January 2004 |
The aims of this study were to compare the renal consequences of two different approaches to blocking the activity of the renin angiotensin system - Angiotensin II antagonism with telmisartan and ACE inhibition with enalapril - in patients with hypertension and concurrent type II diabetes mellitus and diabetic nephropathy.
The study was designed to investigate albumin excretion rates in the short term, and in the longer term, to assess the outcome with respect to maintenance of renal function (GFR) and incidence of clinical endpoints.
Study Hypothesis:
Association of Hypertension and Diabetes Essential hypertension accounts for the majority of hypertension in people with diabetes, particularly in those with type II diabetes, who constitute more than 90% of those with a dual diagnosis of diabetes and hypertension.
Both diabetes and hypertension each confer increased cardiovascular risk, and patients with both conditions have more atherogenic risk factors.
Albumin Excretion as a Therapeutic Marker Microalbuminuria is an early and reliable predictor of diabetic nephropathy in both type I - insulin dependent diabetes mellitus (IDDM) and type II - non insulin dependent diabetes mellitus (NIDDM) patients, nephropathy being characterised by hypertension and an inevitable decline in renal function.
Furthermore, diabetic nephropathy is the single most important cause of end stage renal failure (ESRF) in the western world and over recent years the incidence of ESRF in patients with type II diabetes has dramatically increased.
In addition to predicting nephropathy, in type II diabetes, microalbuminuria also predicts mortality, the major causes of death being related to cardiovascular disease.
Comparison(s):
Selection of an ACE Inhibitor as the Comparative Agent Findings in preclinical studies of animals with diabetes mellitus suggest that ACE inhibitors reduce glomerular damage by one or more mechanisms independent of their antihypertensive effects. Glomerular efferent arteriolar tone is increased in diabetic animals and as a result there is an increase in transcapillary hydraulic pressure. These alterations may decrease the functional integrity of the glomerular capillary wall. In rats with diabetes, the long term administration of an ACE inhibitor diminishes the functional and morphologic evidence of glomerular injury and decreases glomerular transcapillary pressure. Removal of the tonic constrictor effect of angiotensin II on efferent arterioles would be expected to lower glomerular intracapillary pressure while preserving renal plasma flow.
Angiotensin II antagonists appear to be as effective as ACE inhibitors in delaying the progression of renal injury in animal models of diabetes.
Eligibility| Ages Eligible for Study: | 35 Years to 80 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Confirmed diagnosis of type II diabetes:
Exclusion Criteria:
Pre-menopausal women (last menstruation < 1 year prior to start of screening period):
Contacts and Locations| Denmark | |
| Hvidovre Hospital | |
| Hvidovre, Denmark, DK-2650 | |
| Apopleksiafsnittet | |
| Frederiksberg, Denmark, DK-2000 | |
| Gynækologisk/obstetrisk afd. | |
| Kolding, Denmark, 6000 | |
| Medical Dept. B0642 | |
| Hillerød, Denmark, DK-3400 | |
| Boehringer Ingelheim Investigational Site | |
| Frederiksberg C, Denmark, DK-1900 | |
| Lungemedicinsk Forskning | |
| Hellerup, Denmark, DK-2900 | |
| Finland | |
| Boehringer Ingelheim Investigational Site | |
| Hyvinkää, Finland, 05850 | |
| Boehringer Ingelheim Investigational Site | |
| Tampere, Finland, 33520 | |
| Kuopion yliopistollinen sairaala, Keuhkoklinikka | |
| Kuopio, Finland, FI-70211 | |
| Boehringer Ingelheim Investigational Site | |
| Jyväskylä, Finland, FIN-40100 | |
| Boehringer Ingelheim Investigational Site | |
| Riihimäki, Finland, 11100 | |
| Netherlands | |
| Bosch Medicentrum | |
| Den Bosch, Netherlands, 5223 GV | |
| Dept. of Internal Medicine | |
| Utrecht, Netherlands, 3584 CX | |
| Norway | |
| Boehringer Ingelheim Investigational Site | |
| Jessheim, Norway, N-2050 | |
| Boehringer Ingelheim Investigational Site | |
| Arendal, Norway, N-4841 | |
| Hjertelaget Research Foundation | |
| Stavanger, Norway, N-4011 | |
| Boehringer Ingelheim Investigational Site | |
| Skogn, Norway, N-7620 | |
| Sweden | |
| Medicinkliniken | |
| Eksjö, Sweden, 575 81 | |
| Boehringer Ingelheim Investigational Site | |
| Munkedal, Sweden, 455 30 | |
| Medicinkliniken | |
| Helsingborg, Sweden, 251 87 | |
| Boehringer Ingelheim Investigational Site | |
| 573 83, Sweden, Tranås | |
| Boehringer Ingelheim Investigational Site | |
| Helsingborg, Sweden, 254 67 | |
| Samariterhemmets sjukhus | |
| Uppsala, Sweden, 751 25 | |
| Boehringer Ingelheim Investigational Site | |
| Vetlanda, Sweden, 574 28 | |
| Boehringer Ingelheim Investigational Site | |
| Uddevalla, Sweden, 451 40 | |
| United Kingdom | |
| Department of Respiratory Medicine | |
| Birmingham, United Kingdom, B9 5SS | |
| Diabetes Centre | |
| Rugby, United Kingdom, CV22 5PX | |
| Finance Office (Research Unit) | |
| Newcastle-Upon-Tyne, United Kingdom, NE1 7RU | |
| Northampton General Hospital | |
| Northampton, United Kingdom, NN1 5BD | |
| Lucille Packard Children's Health Services at Stanford | |
| Palo Alto, United Kingdom, 94304-5786 | |
| Boehringer Ingelheim Investigational Site | |
| Pontyclun, United Kingdom, CF72 9AA | |
| Boehringer Ingelheim Investigational Site | |
| Northampton, United Kingdom, NN5 7AQ | |
| Boehringer Ingelheim Investigational Site | |
| Atherstone, United Kingdom, CV9 1EU | |
| Boehringer Ingelheim Investigational Site | |
| Barry, United Kingdom, CF62 7EB | |
| Diabetes Centre, | |
| Nuneaton,, United Kingdom, CV10 7DJ | |
| Royal Bournemouth Hospital | |
| Bournemouth, United Kingdom, BH7 7DW | |
| Dept. of Diabetes | |
| Birmingham, United Kingdom, B18 7QH | |
| Study Chair: | Boehringer Ingelheim Study Coordinator | Boehringer Ingelheim Ltd./Bracknell |
More Information
| Study ID Numbers: | 502.236 |
| Study First Received: | January 9, 2006 |
| Last Updated: | September 27, 2009 |
| ClinicalTrials.gov Identifier: | NCT00274118 History of Changes |
| Health Authority: | Denmark: Ethics Committee, Sjaellandsgrade 40DK-2200 CPH; Finland: Ethics Committee, 00029 HUS; Netherlands: Committee Scientifical, 3584 CX Utrecht; Norway: Regional Komite for Medisinsk, 0371 Oslo; Sweden: Forskningsetikkommitteen, 58185 Linkoping |
|
Metabolic Diseases Molecular Mechanisms of Pharmacological Action Diabetes Mellitus Vascular Diseases Endocrine System Diseases Enzyme Inhibitors Cardiovascular Agents Antihypertensive Agents Pharmacologic Actions Protease Inhibitors |
Angiotensin II Type 1 Receptor Blockers Enalapril Enalaprilat Therapeutic Uses Diabetes Mellitus, Type 2 Angiotensin-Converting Enzyme Inhibitors Cardiovascular Diseases Telmisartan Glucose Metabolism Disorders Hypertension |