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Clinical Trials/NCT00233051
NCT00233051
Terminated
Not Applicable

Expression of Inflammatory Mediators in Induced Sputum: A Potential Biomarker of Drug Response in COPD

National Jewish Health1 site in 1 country20 target enrollmentApril 2003

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Chronic Obstructive Pulmonary Disease (COPD)
Sponsor
National Jewish Health
Enrollment
20
Locations
1
Primary Endpoint
Induced Sputum Gene Expression
Status
Terminated
Last Updated
9 years ago

Overview

Brief Summary

The purpose of this research study is to determine whether analysis of genes in sputum is a useful noninvasive technique for measuring response to drugs in patients with COPD.

We propose to use polymerase chain reaction to evaluate gene expression in induced sputum from adult current smokers with moderate COPD, adult former smokers with moderate COPD. This study is designed to determine whether changes in expression of previously-identified inflammatory markers in induced sputum can be detected in response to drug therapy in COPD and to evaluate potential differences in the expression of these markers in adult smokers with and without COPD. Pre- and post-treatment serum will be obtained to facilitate proteomic analysis of therapeutic response as well. Changes in sputum gene expression in response to treatment will be the primary outcome variable in this study. Secondary outcomes will include changes in lung function, as well as changes in induced sputum inflammation. These endpoints will be evaluated before and directly after 6 weeks of randomly-assigned treatment with either salmeterol xinafoate or fluticasone propionate/50mcg salmeterol xinafoate combination DPI bid. Endpoints will be re-evaluated following a 4 week wash-out period.

Registry
clinicaltrials.gov
Start Date
April 2003
End Date
June 2006
Last Updated
9 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Twenty adult subjects ≥ 40 years of age and ≥ 10 pack/year cigarette history will be evaluated.
  • Subjects will be recruited such that one-half are current smokers and one-half are former smokers.
  • All subjects will have COPD (FEV1/FVC \< 70% and FEV1 =\> 40% predicted).
  • Airway hyperresponsiveness and diffusion capacity for carbon monoxide will also be performed to more precisely characterize the physiologic phenotype in these subjects.

Exclusion Criteria

  • Subjects will be excluded if they have used inhaled or systemic corticosteroid or antibiotic use within 6 weeks or if they are currently treated with theophylline.
  • A 6 weeks run off after an upper respiratory infection will be required for qualifying subjects.

Outcomes

Primary Outcomes

Induced Sputum Gene Expression

Secondary Outcomes

  • Lung Function

Study Sites (1)

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