Vitamin E and C to Slow Progression of Common Carotid Artery Plaque Build-Up
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Purpose
This study will evaluate the effects of vitamin E supplementation in retarding the progression of common carotid artery intima-media thickening in African Americans.
| Condition | Intervention | Phase |
|---|---|---|
|
Cardiovascular Diseases Carotid Artery Diseases Intracranial Arteriosclerosis Cerebrovascular Disorders Heart Diseases Vascular Diseases Atherosclerosis |
Drug: Vitamin E Drug: Vitamin C |
Phase 2 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Primary Purpose: Prevention |
| Official Title: | Antioxidants and Prevention of Early Atherosclerosis |
- rate of change in average common carotid artery intima-media thickness (measured over 24 months)
| Study Start Date: | June 1995 |
BACKGROUND:
Evidence from epidemiologic studies, and from one unpublished study, suggests that greater intake of antioxidant vitamins is associated with reduced risk of coronary heart disease and stroke. Findings from an animal model indicate that increased intake of antioxidant vitamins prevents progression of aortic fatty streaks induced by an atherogenic diet, but not from more advanced injury-induced lesions. These observations suggest the hypothesis that increased antioxidant vitamin intake may prevent further progression of early atherosclerosis, possibly by means of reduced susceptibility of low density lipoprotein to oxidative modification and consequent cytotoxic, chemotactic, chemostatic, and unregulated uptake effects.
A new, automated, low-cost, portable ultrasound system for determining intima-media thickness of the common carotid artery makes it feasible to test the primary prevention impact of antioxidant vitamins on early atherosclerosis. Results of two studies at the University of Southern California suggest that the low-density lipoprotein effects on common carotid artery intima-media thickness can be detected by automated methods within 12 to 24 months in small patient samples. Retardation of intima-media thickness progression was achieved in both studies without significant changes in average vessel diameter, which suggests effects on early atherosclerotic lesions.
DESIGN NARRATIVE:
Patients will be screened for carotid intima-media thickness at home or at schools in mobile vans equipped with portable ultrasound equipment. After 12 months, those patients above the age and sex-adjusted 66th percentile at Screen I will be re-screened (Screen II), and those showing the greatest progression in intima-media thickness will be invited to participate in a trial run-in to assess vitamin E compliance. Patients will be randomized to the following four groups: 1) vitamin E (573 mg/day); 2) vitamin C; 3) Vitamin E and C combined; and 4) placebo. Common carotid artery intima-media thickness will be observed by ultrasound at 12- and 24-month follow-ups. The primary outcome is 24-month rate of change in average common carotid artery intima-media thickness.
Eligibility| Ages Eligible for Study: | 35 Years to 59 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- African American
Contacts and Locations
More Information
No publications provided
| ClinicalTrials.gov Identifier: | NCT00000600 History of Changes |
| Other Study ID Numbers: | 106, U01 HL52073 |
| Study First Received: | October 27, 1999 |
| Last Updated: | October 25, 2006 |
| Health Authority: | United States: Federal Government |
Additional relevant MeSH terms:
|
Atherosclerosis Intracranial Arteriosclerosis Cerebrovascular Disorders Carotid Artery Diseases Vascular Diseases Heart Diseases Arteriosclerosis Cardiovascular Diseases Carotid Stenosis Arterial Occlusive Diseases Intracranial Arterial Diseases Brain Diseases Central Nervous System Diseases Nervous System Diseases |
Vitamins Vitamin E Alpha-Tocopherol Tocopherols Tocotrienols Ascorbic Acid Micronutrients Growth Substances Physiological Effects of Drugs Pharmacologic Actions Antioxidants Molecular Mechanisms of Pharmacological Action Protective Agents |
ClinicalTrials.gov processed this record on June 18, 2013