Vitamin C (Ascorbic Acid) |
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Clinical Trial: Gender, Obesity, C-Reactive Protein, and Oxidative Stress
This study is currently recruiting patients.
Purpose
This randomized placebo-controlled trial will test whether supplementing with vitamins C and E can lower markers of inflammation and oxidative stress in healthy adults. We will examine whether one antioxidant vitamin is more effective than another, and whether gender or body fat influence the treatment effects. We will also determine whether gender, body fat, or menopausal status are associated with baseline concentrations of inflammation and oxidative stress markers.
| Condition | Treatment or Intervention |
|---|---|
| Cardiovascular Disease | Drug: Vitamin C Drug: Vitamin E |
MedlinePlus related topics: Heart Diseases; Vascular Diseases
Study Type: Interventional
Study Design: Prevention, Randomized, Double-Blind, Placebo Control, Parallel Assignment, Efficacy Study
Expected Total Enrollment: 400
Study start: April 2004
Eligibility
Ages Eligible for Study: 18 Years and above, Genders Eligible for Study: Both
Accepts Healthy Volunteers
Criteria
Inclusion criteria:
- Nonsmoker and not passively exposed
- Males and females 18 year and older
- Able to take vitamin supplements
- Able to take acetominophen instead of aspirin or NSAIDs during the study
Exclusion criteria:
- Pregnancy or lactation
- History of ever smoking or passive smoke exposure in the last year
- Active liver disease; history of HIV/AIDS, diabetes, kidney stones, hemochromatosis, or autoimmune diseases; heart disease, stroke, or cancer in the last 5 years
- User of prescribed anti-inflammatory or lipid-lowering medications, oral contraceptives, hormone replacement therapy, or blood-thinning drugs
- User of iron supplements or vitamin E at 600 IU per day or more
- Consumption of more than 2 alcoholic beverages per day
Location and Contact Information
California
University of California, Berkeley School of Public Health, Berkeley, California, 94720-7360, United States; Recruiting
Chris Jensen, PhD 510-642-1875 cjensen@berkeley.edu
Gladys Block, PhD, Principal Investigator
More Information
Record last reviewed: March 2005
Last Updated: March 4, 2005
Record first received: March 18, 2004
ClinicalTrials.gov Identifier: NCT00079963
Health Authority: United States: Federal Government
ClinicalTrials.gov processed this record on 2005-04-08
Source: ClinicalTrials.gov
Cache Date: April 9, 2005

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