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| Sponsor: | RWTH Aachen University |
|---|---|
| Collaborators: |
CTCA University of Heidelberg Bayer |
| Information provided by: | RWTH Aachen University |
| ClinicalTrials.gov Identifier: | NCT00559286 |
Purpose
The hypothesis of the presented study is: Telmisartan induces an increase of eNOS activity in RBC resulting in an enhanced intravascular NO bioavailability, an ameliorated RBC deformability and a reduction of RBC and platelet aggregation. This could be a potential mechanism of the improvement of microcirculatory disorders, especially in patients with diabetes mellitus and arterial hypertension, treated with Telmisartan.
| Condition | Intervention | Phase |
|---|---|---|
|
Arterial Hypertension Diabetes Mellitus Type 2 IRC or NIR |
Drug: Telmisartan |
Phase IV |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Parallel Assignment Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor) Primary Purpose: Treatment |
| Official Title: | Influence of the Angiotensin Receptor Blocker Telmisartan on the Red Blood Cell Function and the Microcirculatory Perfusion |
| Estimated Enrollment: | 40 |
| Study Start Date: | December 2007 |
| Study Completion Date: | January 2009 |
| Primary Completion Date: | January 2009 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: A
treatment with 80 mg Telmisartan per day for 30 days
|
Drug: Telmisartan
application of 80mg or 20mg Telmisartan per day for 30 days
|
|
Active Comparator: B
treatment with 20mg Telmisartan per day for 30 days
|
Drug: Telmisartan
application of 80mg or 20mg Telmisartan per day for 30 days
|
Recently, it could be shown that the renin-angiotensin-system (RAS) influences different signal transduction pathways within the red blood cells (RBC). This includes the Na+/H+ exchange activity, the Ca2+-ATP-ase mediated Ca2+efflux, the erythropoietin- dependent production of RBC, the RBC deformability, RBC aggregation and the interaction of RBC and platelets. Recent studies and experiments, done by our group, focus on the oxidative and nitrosative metabolism of NO within the blood. The interactions of the RAS and endothelial NO are well known and described in detail. Based on a wide experience in this research field of NO metabolism, we characterized recently an active endothelial-type NO-synthase in RBC on the biochemical, functional and molecular level. Erythrocyte-derived NO formation serves important regulatory functions essential for adequate passage of blood through the vasculature. Here we aimed to treat patients with diabetes mellitus and arterial hypertension with Telmisartan as an angiotensin receptor antagonist. Efficacy parameters studied in this study should be: i) RBC deformability, RBC aggregation, ii) RBC dependent production of nitric oxide as well as detection of eNOS activity in RBC and iii) indices of microcirculatory perfusion. This project could broaden the view of effects of Telmisartan in the treatment of microcirculatory disorders in patients with diabetes mellitus and arterial hypertension, who exhibit a reduced NO bioavailability and RBC function.
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Male |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Contacts and Locations| Germany | |
| University Hospital | |
| Aachen, NRW, Germany, 52074 | |
| Principal Investigator: | Malte Kelm, MD, Univ.Prof. | Department of Cardiology, Angiology, Pulmonary Diseases and cardiologic critical care |
More Information
| ClinicalTrials.gov Identifier: | NCT00559286 History of Changes |
| Other Study ID Numbers: | AIX-MK-01, EUDRA CT No 2007-002765-12 |
| Study First Received: | November 15, 2007 |
| Last Updated: | January 28, 2009 |
| Health Authority: | Germany: Federal Institute for Drugs and Medical Devices |
|
perfusion microcirculation RBC function NO metabolism AT receptor blocker |
|
Diabetes Mellitus Diabetes Mellitus, Type 2 Hypertension Glucose Metabolism Disorders Metabolic Diseases Endocrine System Diseases Vascular Diseases Cardiovascular Diseases Antihypertensive Agents Telmisartan Angiotensin Receptor Antagonists |
Benzoates Cardiovascular Agents Therapeutic Uses Pharmacologic Actions Angiotensin II Type 1 Receptor Blockers Molecular Mechanisms of Pharmacological Action Angiotensin-Converting Enzyme Inhibitors Protease Inhibitors Enzyme Inhibitors Antifungal Agents Anti-Infective Agents |