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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00948454
Other study ID # 704074
Secondary ID 0775
Status Completed
Phase N/A
First received July 28, 2009
Last updated October 23, 2009
Start date January 2003
Est. completion date June 2006

Study information

Verified date October 2009
Source University of Pennsylvania
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

The current proposal, will elucidate the role of oxidant stress (OS) on arterial function as measured by flow mediated vasodilation. In addition, the investigators will address the hypothesis, that a pro-oxidant might have different degrees of effects on different biological targets, by performing quantitative assessment of the effects of OS on lipids, proteins and DNA.


Recruitment information / eligibility

Status Completed
Enrollment 105
Est. completion date June 2006
Est. primary completion date May 2006
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Chronic smokers (of between 4 and 20 years duration) and non-smokers will be recruited to the GCRC. Smokers will be allocated to a "light" group, smoking 4-10 cigarettes per day and a "heavy" smoking group who smoke 11-20 cigarettes per day.

- Non-smokers will be defined as those with a life time consumption of no more than 20 cigarettes, do not live or work in a smoky atmosphere.

- All individuals will have a normal history and clinical examination, including a normal EKG, urinalysis and serum chemistry, haemogram and negative urinary pregnancy test.

Exclusion Criteria:

- previously suffered an acute major cardiovascular event

- those with a chronic disease

- those taking chronic medication

- those with a history of alcoholism or substance abuse

- Ex-smokers

- Subjects, who have less than or equal to 60% platelet aggregation in response to arachidonic acid

Study Design

Observational Model: Case Control, Time Perspective: Cross-Sectional


Related Conditions & MeSH terms


Locations

Country Name City State
United States University of Pennsylvania Philadelphia Pennsylvania

Sponsors (2)

Lead Sponsor Collaborator
University of Pennsylvania National Institutes of Health (NIH)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary To assess the dose-related effects of cigarette smoking on flow mediated arterial function in humans. Study Day No
Secondary To assess the dose-related effects of cigarette smoking on COX activation. Twice during study day No
Secondary To assess the dose-related effects of cigarette smoking on novel indices of lipid peroxidation, protein oxidation and DNA modification by lipid adducts. Study day No
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