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The Effects of Ramipril on Clinical Symptoms in Patients With Peripheral Arterial Disease
This study has been completed.
Sponsored by: Baker Heart Research Institute
Information provided by: Baker Heart Research Institute
ClinicalTrials.gov Identifier: NCT00168467
  Purpose

One important clinical challenge in older individuals is maintaining mobility in the absence of pain. Peripheral arterial disease affects up to 12% of adults over 50 and impairs quality of life due to intermittent claudication causing pain and limiting mobility.

Conventional therapies have only modest effect in improving symptoms. We hypothesise that angiotensin converting enzyme inhibition (with ramipril), which causes arterial vasodilation, also improves clinical symptoms in patients with peripheral arterial disease.


Condition Intervention Phase
Peripheral Arterial Disease
Drug: Ramipril
Phase IV

Drug Information available for: Ramipril
U.S. FDA Resources
Study Type: Interventional
Study Design: Treatment, Randomized, Double-Blind, Placebo Control, Parallel Assignment
Official Title: The Effects of Ramipril on Clinical Symptoms in Patients With Peripheral Arterial Disease

Further study details as provided by Baker Heart Research Institute:

Primary Outcome Measures:
  • Time to onset of claudication
  • Total exercise time during a standard treadmill test
  • Walking ability measured using the standard Walking Impairment Questionnaire

Secondary Outcome Measures:
  • Leg Blood Flow using Duplex Ultrasound

Estimated Enrollment: 40
  Eligibility

Ages Eligible for Study:   up to 70 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Ankle-brachial index of <0.9 at rest in at least one leg
  • History of intermittent claudication (unilateral or bilateral) which was stable for 6 months
  • Evidence of superficial femoral artery stenosis or occlusion on duplex scan
  • Blood pressure <=160/90 mmHg
  • Stable medication regimen for at least 6 months and not previously treated with ACE inhibitors

Exclusion Criteria:

  • Limiting coronary artery disease
  • Renal Failure
  • History of hypertension
  • History of type 2 diabetes mellitus
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00168467

Locations
Australia, Victoria
Alfred Hospital
Melbourne, Victoria, Australia, 3004
Sponsors and Collaborators
Baker Heart Research Institute
Investigators
Principal Investigator: Bronwyn A Kingwell, PhD Baker Heart Research Institute
  More Information

Publications of Results:
Study ID Numbers: 20/03
Study First Received: September 9, 2005
Last Updated: July 20, 2006
ClinicalTrials.gov Identifier: NCT00168467  
Health Authority: Australia: Department of Health and Ageing Therapeutic Goods Administration

Study placed in the following topic categories:
Peripheral Vascular Diseases
Vascular Diseases
Ramipril

Additional relevant MeSH terms:
Molecular Mechanisms of Pharmacological Action
Therapeutic Uses
Angiotensin-Converting Enzyme Inhibitors
Enzyme Inhibitors
Cardiovascular Diseases
Cardiovascular Agents
Antihypertensive Agents
Pharmacologic Actions
Protease Inhibitors

ClinicalTrials.gov processed this record on January 13, 2009