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Sponsors and Collaborators: |
University of Virginia National Institutes of Health (NIH) |
Information provided by: | University of Virginia |
ClinicalTrials.gov Identifier: | NCT00587678 |
The purpose of this study is to develop new ways of imaging fatty blockages in the leg arteries to improve upon techniques used now and to develop new ways of understanding how new treatments may affect the disease.
Condition | Intervention |
Peripheral Artery Disease |
Drug: Simvastatin Drug: Ezetimibe Drug: Simvastatin/Ezetimibe |
ChemIDplus related topics: | Simvastatin Ezetimibe Vytorin |
Study Type: | Interventional |
Study Design: | Treatment, Randomized, Double Blind (Subject, Investigator, Outcomes Assessor), Historical Control, Parallel Assignment, Efficacy Study |
Official Title: | Comprehensive Magnetic Resonance of Peripheral Arterial Disease |
Enrollment: | 87 |
Study Start Date: | January 2006 |
Estimated Study Completion Date: | October 2009 |
Estimated Primary Completion Date: | October 2009 (Final data collection date for primary outcome measure) |
Arms | Assigned Interventions |
R: Experimental
Patients are imaged at baseline and randomized to Simvistatin 40 mg daily or Simvistatin 40mg/Zetia 10mg daily for 2 years
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Drug: Simvastatin
40mg
Drug: Simvastatin/Ezetimibe
40mg/10mg
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Z: Experimental
Patients are imaged at baseline and treated with ezetimibe 10mg for 2 years.
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Drug: Ezetimibe
10mg
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Ages Eligible for Study: | 30 Years to 85 Years |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Patients age 30-85 referred to the vascular imaging laboratory with documented evidence of peripheral arterial disease (0.4<ABI<0.9) 96 Normal healthy subjects ages 30-85
Exclusion Criteria:
Age<30, >85
GFR less than 45mL/min based on a serum creatinine drawn within 90 days of the MRI:
Pregnancy Contraindications to a magnetic resonance examination
United States, Virginia | |||||
University of Virgina Health System | |||||
Charlottesville, Virginia, United States, 22908 |
University of Virginia |
National Institutes of Health (NIH) |
Principal Investigator: | Christopher M Kramer, M.D. | University of Virginia Health System |
Responsible Party: | University of Virginia Health System ( Christopher Kramer M.D. ) |
Study ID Numbers: | IRB HSR 10387, R01 HL75792 |
First Received: | December 21, 2007 |
Last Updated: | June 4, 2008 |
ClinicalTrials.gov Identifier: | NCT00587678 |
Health Authority: | United States: Institutional Review Board |
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