Expired Study
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Berkeley, California 94720


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.


Study summary:

Participants will be given 1000 mg vitamin C or 800 IU vitamin E daily for 60 days.


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


NCT ID:

NCT00079963


Primary Contact:

Principal Investigator
Gladys Block, Ph.D.
University of California at Berkeley


Backup Contact:

N/A


Location Contact:

Berkeley, California 94720
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: October 09, 2019

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