Carotid Atherosclerosis Regression at Magnetic Resonance Assessment.
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Purpose
The primary objective of this randomized, double blind, placebo controlled pilot study is to determine if therapies aimed at lowering LDL cholesterol (HMGCoA reductase inhibitor – simvastatin) or increasing HDL cholesterol (Niaspan) will induce regression of carotid atherosclerotic plaque in vivo using MRI imaging techniques. MR plaque morphology at baseline will be compared to that after 6 and 12 months of therapy and changes in MR characteristics will be compared to changes in lipoprotein parameters and urinary isoprostanes. The effect of moderate LDL reduction, aggressive LDL reduction and the combination of aggressive LDL reduction and HDL elevation on MRI plaque characteristics will be compared by randomly assigning subjects (n=69) with carotid disease (>30% stenosis by ultrasound criteria) to one of three treatment arms;
- Simvastatin 20 mg daily and placebo Niaspan (n=23)
- Simvastatin 80 mg daily and placebo Niaspan (n=23)
- Simvastatin 20 mg daily and active Niaspan (n=23) Treatment group 2 and 3 will have roughly equivalent LDL lowering because of the synergistic LDL lowering effect of the combination of simvastatin and Niaspan.
| Condition | Intervention | Phase |
|---|---|---|
|
Established Carotid Atherosclerosis |
Drug: Niacin/simvastatin compared to simvastatin alone at 2 doses |
Phase 4 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Pharmacodynamics Study Intervention Model: Parallel Assignment Masking: Double-Blind Primary Purpose: Treatment |
| Official Title: | Magnetic Resonance Characterization of Carotid Atherosclerotic Plaque in Vivo: Effect of High Density Lipoprotein Elevation on Plaque Morphology |
- Change in MRI estimates of carotid atherosclerosis
- Change in lipoproteins and inflammatory markers
| Estimated Enrollment: | 69 |
| Study Start Date: | January 2000 |
| Estimated Study Completion Date: | September 2005 |
Show Detailed Description
Eligibility| Ages Eligible for Study: | 18 Years to 90 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- Age > 18 and < 90 years
- Capacity for giving written informed consent
- Carotid stenosis of > 30% by ultrasound criteria
- LDL cholesterol level of > 100mg/dl
- Systolic BP < 170 and diastolic BP < 100 under resting conditions
- Negative pregnancy test if female of child-bearing potential
Exclusion Criteria:
- Recent (< 3 months) history of stroke, transient ischemic attack, myocardial infarction, unstable angina or critical limb ischemia
- Contraindications to MRI (claustrophobia, presence of pacemakers, defibrillators, metal foreign bodies)
- History of side effect/adverse reaction on HMGCoA reductase inhibitor
- Niaspan or niacin
- Poorly controlled diabetes (HbA1c > 8%)
- History of myositis, liver disease or abnormal LFTs
- Need for combination therapy for the control of severe hyperlipidemia
- Abnormal LFT (> 2 fold upper limit normal)
- Active infection or malignancy
Contacts and Locations
More Information
No publications provided
| ClinicalTrials.gov Identifier: | NCT00307307 History of Changes |
| Other Study ID Numbers: | CARMA |
| Study First Received: | March 24, 2006 |
| Last Updated: | May 18, 2006 |
| Health Authority: | United States: Institutional Review Board |
Keywords provided by University of Pennsylvania:
|
atherosclerosis HDL cholesterol niacin MR imaging |
Additional relevant MeSH terms:
|
Atherosclerosis Carotid Artery Diseases Arteriosclerosis Arterial Occlusive Diseases Vascular Diseases Cardiovascular Diseases Cerebrovascular Disorders Brain Diseases Central Nervous System Diseases Nervous System Diseases Niacin Simvastatin Vasodilator Agents Cardiovascular Agents |
Therapeutic Uses Pharmacologic Actions Hypolipidemic Agents Antimetabolites Molecular Mechanisms of Pharmacological Action Lipid Regulating Agents Vitamin B Complex Vitamins Micronutrients Growth Substances Physiological Effects of Drugs Hydroxymethylglutaryl-CoA Reductase Inhibitors Anticholesteremic Agents Enzyme Inhibitors |
ClinicalTrials.gov processed this record on May 19, 2013