Skip to content

Obesity, Inflammation and Oxidative Stress

Obesity, Inflammation and Oxidative Stress

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01028976
Enrollment
512
Registered
2009-12-09
Start date
2010-01-31
Completion date
2012-07-31
Last updated
2015-12-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

C-reactive Protein, Inflammation, Obesity, Oxidative Stress

Keywords

randomized controlled trial, primary prevention, Vitamin C, Antioxidants, C-reactive protein, inflammation, anti-inflammatory agents, obesity

Brief summary

The purpose of this study is to determine whether or not Vitamin C (1000 mg/day) can reduce markers of inflammation, especially C-reactive protein (CRP), in obese persons with baseline CRP greater than 1 mg/dl.

Detailed description

The long-term objective of this project is to identify nutritional factors that can reduce the inflammatory component of obesity. Therapies to minimize obesity-related comorbidities are needed, and targeting inflammation may help slow the progression of obesity towards cardiovascular disease and insulin resistance. Adipose tissue is a source of inflammatory cytokines, and obesity is now viewed as a chronic, low-grade inflammatory state. Inflammation itself is a contributor to the chronic diseases associated with obesity. C-reactive protein (CRP) is a key marker of inflammation, and as a downstream marker it provides functional integration of upstream cytokine activation associated with inflammation. We have previously shown that vitamin C, but not vitamin E, reduces CRP in active and passive smokers and in nonsmokers. The reduction is seen primarily in persons with CRP ≥1.0 mg/L, the CDC threshold for elevated cardiovascular disease risk. We also found that 75% of obese nonsmokers had CRP ≥1.0 mg/L. The important observation of reduction in elevated CRP by vitamin C now needs to be confirmed in a rigorous study with adequate sample size, to permit justifiable conclusions about the potential usefulness of this agent in reducing inflammation in the obese. We will conduct a placebo-controlled, randomized trial in 552 healthy obese individuals with moderate CRP elevations (CRP ≥1.0 mg/L). Participants will be randomized to either 1000 mg/day vitamin C or placebo for a period of 2 months. We will also characterize the pathways through which this effect takes place by measuring cytokines and oxidative stress. This project is important because if our previous finding is confirmed in this population, it could offer a low-cost alternative to use of statins to reduce inflammation in persons without other risk factors.

Interventions

DIETARY_SUPPLEMENTVitamin C (ascorbic acid)

1000 mg/day (two 500-mg tablets), 8 weeks

DIETARY_SUPPLEMENTPlacebo tablet

Placebo tablet (two 500-mg tablets), 8 weeks

Sponsors

Kaiser Permanente
CollaboratorOTHER
University of California, Berkeley
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* BMI ≥ 30 * hsCRP ≥ 1 mg/L * Age 18+ * Member of Kaiser Permanente Health Plan of Northern California

Exclusion criteria

* Smoker * Unwilling to discontinue vitamin supplements for study duration * Unwilling/unable to use acetaminophen in place of OTC anti-inflammatory medications * Use of certain medications * History of certain medical conditions

Design outcomes

Primary

MeasureTime frame
high-sensitivity C-reactive proteinAfter 8 weeks of intervention

Secondary

MeasureTime frame
CRP-related markers of inflammation and oxidative stress, including cytokines and F2-isoprostanes.After 8 weeks of intervention.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026