Interleukin (IL)-13 as a Marker in Pediatrics Asthma

NCT ID: NCT00968305

Last Updated: 2009-08-28

Study Results

Results pending

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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Recruitment Status

COMPLETED

Total Enrollment

19 participants

Study Classification

OBSERVATIONAL

Study Start Date

2008-11-30

Study Completion Date

2009-08-31

Brief Summary

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Asthma is a very common childhood chronic illness and is generally more severe in African Americans. The investigators attempted to determine whether a specific immune marker is associated with lung function and asthma severity.

Detailed Description

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This study examined the relationship between Interleukin (IL)-13 from phytohemagglutinin-activated polymorphonuclear blood cells and asthma severity, lung function (measured as FEV1%), and total serum IgE levels in African American children with clinically diagnosed asthma

Conditions

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Asthma

Keywords

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African American children with stable asthma Asthma severity Interleukin 13 from PHA stimulated PBMC Lung function (FEV1%) Total serum IgE Pediatrics

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

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

* African-American race, born in the U.S.
* Age 8-15 years
* Clinical diagnosis of asthma
* Subject is able to understand and follow verbal instructions in English

Exclusion Criteria

* Asthma exacerbation in the 4 weeks preceding the research visit
* 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)
Minimum Eligible Age

8 Years

Maximum Eligible Age

15 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Rush University Medical Center

OTHER

Sponsor Role lead

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

Site Status

Countries

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United States

Other Identifiers

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L06121901

Identifier Type: -

Identifier Source: org_study_id