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Compare Effectiveness of Eplerenone Vs Atenolol in Reversing the Remodelling Resistance Arteries in Subjects with HT - Article


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Atenolol

Tenormin 




Clinical Trial: Compare Effectiveness of Eplerenone Vs Atenolol in Reversing the Remodelling Resistance Arteries in Subjects with HT

This study is currently recruiting patients.
Verified by Pfizer September 2005

Sponsors and Collaborators: Pfizer
Pfizer Canada Inc.
Information provided by: Pfizer
ClinicalTrials.gov Identifier: NCT00147563

Purpose

To investigate the impact of antihypertensive therapy with the selective mineralocorticoid receptor blocker, eplerenone, on small resistance artery remodeling, compared to the effect of equivalent blood pressure control achieved with a b-blocker, atenolol.
Condition Intervention Phase
Hypertension
 Drug: Eplerenone
Phase III

MedlinePlus related topics:  High Blood Pressure

Study Type: Interventional
Study Design: Treatment, Non-Randomized, Double-Blind, Active Control, Parallel Assignment, Efficacy Study

Official Title: A Double-Blind, Parallel Design Study to Compare the Effectiveness of Eplerenone Versus Atenolol in Reversing the Remodeling of Resistance Arteries in Subjects with Mild to Moderate Primary Hypertension

Further Study Details: 
Primary Outcomes: The change from baseline to week 52 in the media/lumen ratio and the maximum % relaxation response to acetylcholine of gluteal subcutaneous resistance vessels, measured from the gluteal biopsy.
Secondary Outcomes: Will be done for both the Intent to Treat and per protocol populations, and use both the LOCF and OC methods
Expected Total Enrollment:  34

Study start: October 2003

Eligibility

Ages Eligible for Study:  30 Years   -   70 Years,  Genders Eligible for Study:  Both
Criteria

Inclusion Criteria:

  • Pt with essential hypertension who have never been treated or untreated within the previous 6 months

Exclusion Criteria:

  • History of Malignant Hypertension
  • Sitting diastolic blood pressure > 115mmHg or sitting Systolic blood pressure > 200mmHg

Location and Contact Information

Please refer to this study by ClinicalTrials.gov identifier  NCT00147563

Pfizer CT.gov Call Center      1-800-718-1021 
Mona Maroun      514-693-4527    mona.maroun@pfizer.com

Canada, Quebec
      Pfizer Investigational Site, Montreal,  Quebec,  H2W 1R7,  Canada; Recruiting

Study chairs or principal investigators

Pfizer CT.gov Call Center,  Study Director,  Pfizer   

More Information

Study ID Numbers:  EPLA-0501-077
Last Updated:  September 6, 2005
Record first received:  September 2, 2005
ClinicalTrials.gov Identifier:  NCT00147563
Health Authority: United States: Food and Drug Administration
ClinicalTrials.gov processed this record on 2005-09-13

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Page Updated: October 3, 2005
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