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Gender, Obesity, C-Reactive Protein, and Oxidative Stress - Article


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Vitamin C (Ascorbic Acid)

 




Clinical Trial: Gender, Obesity, C-Reactive Protein, and Oxidative Stress

This study is currently recruiting patients.

Sponsored by: National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Information provided by: National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

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

Further Study Details: 

Expected Total Enrollment:  400

Study start: April 2004

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

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
Gladys Block, PhD  510-643-7896    gblock@berkeley.edu 
Chris Jensen, PhD  510-642-1875    cjensen@berkeley.edu 
Gladys Block, PhD,  Principal Investigator

More Information

Study ID Numbers:  62378DK
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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December 6, 2009



Page Updated: January 17, 2009
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