Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
19 participants
OBSERVATIONAL
2008-11-30
2009-08-31
Brief Summary
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Detailed Description
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Conditions
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Keywords
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Study Design
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CASE_ONLY
CROSS_SECTIONAL
Study Groups
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Children with asthma
African American children with clinically diagnosed stable asthma
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Age 8-15 years
* Clinical diagnosis of asthma
* Subject is able to understand and follow verbal instructions in English
Exclusion Criteria
* Oral/IV steroid use in the 4 weeks preceding the research visit
* Upper or lower respiratory tract infection in the 4 weeks preceding the research visit
* Antibiotic use in the 4 weeks preceding the research visit
* Use of a short-acting bronchodilator during the 6 hours prior to spirometry (lung function testing)
* Use of a long-acting bronchodilator during the 12 hours prior to spirometry (lung function testing)
8 Years
15 Years
ALL
No
Sponsors
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Rush University Medical Center
OTHER
Responsible Party
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Department of Immunology and Microbiology, Rush University Medical Center
Principal Investigators
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Byung H Yu, MD
Role: PRINCIPAL_INVESTIGATOR
Rush University Medical Center, Department of Immunology and Microbiology
Locations
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Rush University Medical Center; Clinic: University Consultants in Allergy and Immunology
Chicago, Illinois, United States
Countries
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Other Identifiers
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L06121901
Identifier Type: -
Identifier Source: org_study_id