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Effect of Short Term Atorvastatin Treatment,80mg/Day on Early Regression of Carotid Artery Atherosclerotic Lesions

Phase 3 Study of Atorvastatin Effects on Carotid Atherosclerosis

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00640744
Acronym
DCAT
Enrollment
12
Registered
2008-03-21
Start date
2006-02-28
Completion date
2010-02-28
Last updated
2010-12-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Atherosclerosis

Keywords

Atherogenesis, Atheroma, Arteriosclerosis

Brief summary

Atherosclerosis is a disease in which the blood vessels become blocked by plaques (consisting of fat, calcification, and fibrous tissue), reducing blood flow to vital organs and tissues.Blockage of the carotid arteries in the neck is a major cause of stroke. One way of treating carotid atherosclerosis is with cholesterol-lowering drugs called statins. Statins have been shown to reduce the risk of coronary heart disease by 24-40% and risk pf stroke by 11-30%.The purpose of this study is to determine if short term treatment with atorvastatin causes early favorable changes in the plaques that block blood flow through the carotid arteries. These changes can be assessed 1) by taking pictures of the carotid arteries with MRI and Ultrasound before and after statin treatment, and 2) by special studies of the plaques removed from the carotid arteries by surgery.

Detailed description

Candidates for bilateral carotid endarterectomy (CEA) who meet study criteria will provide informed consent before their randomization. Before the first CEA, the patient will have MRI, US, and EBCT exams of both carotids. The most occlusive plaque will be resected at the first CEA. The patient will then receive atorvastatin 80 mg/day for 3 months. Then the second CEA will be performed. Six weeks after the second CEA, the patient will have another MRI, US, and EBCT exam and at 6, 12, and 18 months thereafter. This protocol will allow comparison of the characteristics of the plaque that has been exposed to drug vs the plaque that has not been exposed. It will also allow monitoring the effect of drug on restenosis after surgery.

Interventions

DRUGAtorvastatin

Atorvastatin 80 mg tablet/day for 3 months

Sponsors

Pfizer
CollaboratorINDUSTRY
Baylor College of Medicine
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

* Men or women * \>18 yrs old * Expected to have an endarterectomy on each carotid artery * No contraindications for atorvastatin * Stable cardiovascular health * Lipid lowering treatment less than 6 mo duration * Diabetic included if diabetes is controlled * Patient is not claustrophobic * Patient has evaluable carotid plaques.

Exclusion criteria

* Patient has had previous carotid endarterectomy,stenting, or other procedure * Unstable cardiovascular status * Hypersensitivity to statin therapy * Neck anatomy preventing acquiring bilateral evaluable plaques * Weight over 285 lbs.

Design outcomes

Primary

MeasureTime frame
Changes in carotid plaque composition as assessed by MRI and histology3 months

Secondary

MeasureTime frame
Changes content of cells, proteins and genes in carotid plaque3 months
Changes in content of selected proteins and their encoding genes in carotid plaques3 months

Countries

United States

Contacts

Primary ContactWilliam Insull, M.D.
winsull@bcm.tmc.edu713-798-4128
Backup ContactAddison Taylor, MD/PhD
ataylor@bcm.tmc.edu713-798-4721

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026