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BVAIT: B-Vitamin Atherosclerosis Intervention Trial - Article


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Vitamin C (Ascorbic Acid)

 




Clinical Trial: BVAIT: B-Vitamin Atherosclerosis Intervention Trial

This study is no longer recruiting patients.

Sponsored by: National Institute on Aging (NIA)
Information provided by: National Institute on Aging (NIA)

Purpose

The purpose of this study is to examine whether vitamin B supplementation will reduce the progression of early atherosclerosis in individuals over 40 years old and without clinical evidence of cardiovascular disease (CVD).
Condition Intervention Phase
Atherosclerosis
 Drug: folic acid
 Drug: vitamin B12
 Drug: vitamin B6
Phase II
Phase III

MedlinePlus related topics:  Vascular Diseases

Study Type: Interventional
Study Design: Treatment, Randomized, Double-Blind, Placebo Control, Parallel Assignment, Efficacy Study

Official Title: B-Vitamin Atherosclerosis Intervention Trial (BVAIT)

Further Study Details: 
Primary Outcomes: rate of change of distal common carotid artery (CCA) far wall intima-media thickness (IMT)
Secondary Outcomes: change in coronary and abdominal aortic calcification; neurocognitive change
Expected Total Enrollment:  506

Study start: November 2000;  Study completion: June 2005

The primary hypothesis to be tested is that daily vitamin B supplementation reduces progression of early atherosclerosis. Ultrasonography will be used to measure the rate of change in the thickness of the carotid artery and CT will be used to measure coronary and aortic calcium. The beneficial effects of vitamin B supplementation are expected to occur with or without a change in LDL-C levels.

A total of 506 men and women will be randomized to receive either 1) vitamin B supplementation consisting of folic acid 5mg, vitamin B12 0.4mg, and vitamin B6 50mg, or 2) a matching placebo. Participants will receive ultrasonography at baseline and every 6 months for 2.5 to 4.5 years, and CT scan at baseline and end of study (2.5 to 4.5 years).

Eligibility

Ages Eligible for Study:  40 Years and above,  Genders Eligible for Study:  Both

Accepts Healthy Volunteers

Criteria

Inclusion Criteria:

  • Male or female (postmenopausal)
  • 40 years or older
  • Fasting plasma homocysteine 8.5 micromoles per liter (µmol/L) or greater

Exclusion Criteria:

  • Any clinical signs or symptoms of cardiovascular disease (CVD)
  • Diabetes mellitus or fasting serum glucose 140 mg/dL or greater
  • Triglyceride (TG) levels 500mg/dL or greater
  • Serum creatinine greater than 1.6 mg/dL
  • Uncontrolled hypertension (systolic blood pressure 160 mmHg or greater and/or diastolic blood pressure 100 mmHg or greater)
  • Thyroid disease (untreated)
  • Life threatening disease with prognosis less than 5 years
  • Alcohol intake greater than 5 drinks per day (1 drink = 1 1/2 oz distilled spirits, 4 oz wine, or 12 oz beer) or substance abuse (intravenous drug use, cocaine use)

Location Information


California
      Atherosclerosis Research Unit, Division of Cardiovascular Medicine, Department of Medicine, Los Angeles,  California,  90033,  United States

Study chairs or principal investigators

Howard N. Hodis, MD,  Principal Investigator,  University of California, Atherosclerosis Research Unit, Division of Cardiovascular Medicine, Department of Medicine   

More Information

Study ID Numbers:  AG0024; R01AG017160
Record last reviewed:  June 2005
Last Updated:  June 16, 2005
Record first received:  June 14, 2005
ClinicalTrials.gov Identifier:  NCT00114400
Health Authority: United States: Federal Government
ClinicalTrials.gov processed this record on 2005-06-21


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December 5, 2009



Page Updated: January 17, 2009
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