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Irbesartan Effects on Endothelial Dysfunction in Hypertensive Type II Diabetic Patients Comparing Atenolol (IREDIS)
This study has been completed.
Sponsored by: Sanofi-Aventis
Information provided by: Sanofi-Aventis
ClinicalTrials.gov Identifier: NCT00549133
  Purpose

To show that Irbesartan improves endothelial dysfunction and the procoagulant state which are thought to be the possible mechanisms, inducing a generalized vasculopathy associated with microalbuminuria and vascular events in type II diabetic hypertensive patients


Condition Intervention Phase
Hypertension
Diabetes Mellitus Type 2
Drug: Irbesartan
Phase IV

MedlinePlus related topics: Diabetes High Blood Pressure
Drug Information available for: Atenolol Irbesartan
U.S. FDA Resources
Study Type: Interventional
Study Design: Treatment, Randomized, Open Label, Active Control, Single Group Assignment, Safety/Efficacy Study
Official Title: Irbesartan Effects on Endothelial Dysfunction in Hypertensive Type II Diabetic Patients Comparing Atenolol

Further study details as provided by Sanofi-Aventis:

Primary Outcome Measures:
  • Evaluation of the effect of irbesartan on nitric oxide (NO), which has key role in the endothelial dysfunction and the development of pressure vasomotor response, compared to standard therapy (atenolol)

Secondary Outcome Measures:
  • Evaluation of the effect of irbesartan on chronic inflammatory process and tendency for procoagulation, associated with endothelial dysfunction, compared to atenolol.

Enrollment: 44
Study Start Date: October 2003
Study Completion Date: April 2005
  Eligibility

Ages Eligible for Study:   40 Years to 65 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • non insulin dependent type II manifest diabetes with glycosilated HbA1c levels over %6.5-8
  • mild to moderate hypertension stage I and stage II according to ESC-ESH 2003 (140-180 mmHg)

Exclusion Criteria:

  • congestive heart failure
  • azotemia
  • insulin dependent diabetes
  • liver insufficiency
  • pregnancy
  • cancer

The above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.

  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00549133

Locations
Turkey
Sanofi-Aventis
Istanbul, Turkey
Sponsors and Collaborators
Sanofi-Aventis
Investigators
Study Director: Edibe Taylan Sanofi-Aventis
  More Information

clinicalstudyresults.org  This link exits the ClinicalTrials.gov site

Study ID Numbers: L_9130
Study First Received: October 24, 2007
Last Updated: October 24, 2007
ClinicalTrials.gov Identifier: NCT00549133  
Health Authority: Turkey: Ministry of Health

Keywords provided by Sanofi-Aventis:
Microalbuminaria in hypertensive patients with type II diabetes mellitus

Study placed in the following topic categories:
Metabolic Diseases
Diabetes Mellitus, Type 2
Irbesartan
Vascular Diseases
Diabetes Mellitus
Endocrine System Diseases
Endocrinopathy
Angiotensin II
Atenolol
Metabolic disorder
Glucose Metabolism Disorders
Hypertension

Additional relevant MeSH terms:
Angiotensin II Type 1 Receptor Blockers
Molecular Mechanisms of Pharmacological Action
Therapeutic Uses
Cardiovascular Diseases
Cardiovascular Agents
Antihypertensive Agents
Pharmacologic Actions

ClinicalTrials.gov processed this record on January 15, 2009