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Avoiding Cardiovascular Events through Combination therapy in patients with Systolic Hypertension ACCOMPLISH - Article


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Telmisartan and Hydrochlorothiazide

Micardis HCT



Clinical Trial: Avoiding Cardiovascular Events through Combination therapy in patients with Systolic Hypertension ACCOMPLISH

This study is currently recruiting patients.

Sponsored by: Novartis Pharmaceuticals
Information provided by: Novartis Pharmaceuticals

Purpose

A study of two drugs, Lotrel (amlodipine/benazepril) and benazepril/HCTZ, for effectiveness in reducing heart disease and deaths from heart attacks.

Condition Treatment or Intervention Phase
Heart Disease
 Drug: Lotrel (benazepril/amlodipine)
 Drug: benazepril plus hydrochlorothiazide
Phase III

MedlinePlus related topics:  Heart Diseases;   Heart Diseases--Prevention

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

Official Title: Comparison of the Safety and Effectiveness of Lotrel and Benazapril+HCTZ in Reducing Heart Disease and Heart Attacks

Further Study Details: 
Primary Outcomes: Cardiovascular morbidity; Cardiovascular mortality
Expected Total Enrollment:  12600

Study start: October 2003

Eligibility

Ages Eligible for Study:  55 Years and above,  Genders Eligible for Study:  Both

Criteria

Inclusion Criteria:

  • Adults with high risk hypertension.
  • At least 55 years of age.
  • Have elevated blood pressure and at least one other cardiovascular disease or diabetes or evidence of damage to the kidneys, brain, blood vessels or heart as defined in the protocol.

Exclusion Criteria:

  • Allergy to any of the drugs administered in this trial.
  • Selected laboratory tests.

More details provided by the study contact person.


Location and Contact Information

Malcolm Bohm      862-778-6345    malcolm.bohm@pharma.novartis.com

New Jersey
      Malcolm Bohm, East Hanover,  New Jersey,  07936,  United States; Recruiting

More Information

Study ID Numbers:  CCIB002I2301
Record last reviewed:  December 2004
Last Updated:  December 21, 2004
Record first received:  November 30, 2004
ClinicalTrials.gov Identifier:  NCT00097864
Health Authority: United States: Food and Drug Administration
ClinicalTrials.gov processed this record on 2005-04-08


Source: ClinicalTrials.gov
Cache Date: April 8, 2005

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November 18, 2008



Page Updated: June 1, 2005
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