Carotid Atherosclerosis Clinical Trial
Official title:
Short Term Carotid Plaque Regression in Patients With Atherosclerotic Disease Taking Statins Assessed by High Field MRI
Verified date | August 2015 |
Source | Medical College of Wisconsin |
Contact | n/a |
Is FDA regulated | No |
Health authority | United States: Institutional Review Board |
Study type | Observational |
The purpose of the study is to determine if short term (6 months) treatment with statins to lower low-density lipoprotein (LDL) in vascular disease patients with carotid plaque will be associated with a measurable reduction in carotid plaque volume using 3 Tesla MRI. The researchers will correlate the change in plaque volume to degree of LDL lowering. The researchers will also study if brief treatment will lead to change in plaque composition. The researchers will compare the change in plaque volume measured by 3T MRI with plaque burden measured by ultrasound.
Status | Withdrawn |
Enrollment | 0 |
Est. completion date | February 2009 |
Est. primary completion date | February 2009 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 21 Years and older |
Eligibility |
Inclusion criteria: - Adult (> 21 years old) patients. - Diagnosed with coronary artery disease or suspected cerebrovascular accident. - For dose increased subjects, patients whose statin dose or LDL lowering therapy is doubled or increased from standard dose to high dose (see table). - For dose maintained subjects, patients whose statin dose or LDL lowering therapy is maintained at standard dose (see table). - Standard Dose (reported LDL? < 40% from literature) - Drug Daily Dose/s: (md/day) - atorvastatin 10 - simvastatin 5, 10, 20 - pravastatin 10, 20, 40, 80 - fluvastatin 20, 40, 80 - lovastatin 10, 20, 40 - High Dose (reported LDL? > 40% from literature) - Drug Daily Dose/s (mg/day) - atorvastatin 40, 80 - simvastatin 40, 80 - lovastatin 80 - rosuvastatin 5, 10, 20, 40 - Addition of non-statin lipid transfer (tx) (e.g., ezetimibe, fibrate, niacin) to standard statin dose Exclusion criteria: - severe claustrophobia causing inability to undergo MRI implanted ferromagnetic materials (pacemakers, defibrillators, TENS units, aneurysm clips, etc.) that are not suitable for MRI in the clinical setting - patients anticipated to undergo carotid stenting or surgery in next 6 months - patients unable to lie flat for 1 hour - patients requiring supplemental oxygen - pregnant women - patients who could not be followed up for 6 months |
Observational Model: Cohort, Time Perspective: Prospective
Country | Name | City | State |
---|---|---|---|
United States | Medical College of Wisconsin/Froedtert Memorial and Lutheran Hospital | Milwaukee | Wisconsin |
Lead Sponsor | Collaborator |
---|---|
Medical College of Wisconsin |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in carotid artery plaque volume assessed by carotid MRI at 6 months | 6 months | No | |
Secondary | Change in carotid intima media thickness on ultrasound at 6 months | 6 months | No | |
Secondary | Change in plaque composition by carotid MRI at 6 months | 6 months | No | |
Secondary | Change in inflammatory markers at 6 months | 6 months | No | |
Secondary | Change in regional wall shear stress in the carotid artery | 6 months | No |
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