Lung Function and Structure in Healthy Infants and Infants With Recurrent Wheezing
NCT ID: NCT00507676
Last Updated: 2012-03-30
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
220 participants
OBSERVATIONAL
2000-10-31
2007-12-31
Brief Summary
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Detailed Description
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It is not known whether infants with recurrent wheezing have persistent airway narrowing when not acutely symptomatic, and whether airway function in these infants is related to ETS exposure, Fm Asthma, and male gender. When recurrently wheezy infants are asymptomatic, airway function may be low or normal, and low airway function may be fixed or reversible with a bronchodilator. It is important to determine whether these infants have functional and structural abnormalities when they are not acutely symptomatic, and to determine how lung structure relates to lung function. Only then can we design effective therapeutic interventions for recurrently symptomatic infants, as well as, design early intervention strategies.
The Specific aims of this project are:
Specific Aim # 1: To determine whether asymptomatic groups of infants at high risk for wheezing (Environmental tobacco smoke (ETS) exposure, Fm Asthma, male Gender) have fixed or reversible airway narrowing.
Specific Aim # 2: To determine the relative contributions of fixed and reversible airway narrowing in infants with recurrent symptomatic wheezing, and to determine whether fixed and reversible airway narrowing is related to ETS exposure, Fm Asthma, and male Gender.
We propose to answer these important questions of lung function and structure in infants using state of the art methodologies
Conditions
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Keywords
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Study Design
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CASE_CONTROL
PROSPECTIVE
Study Groups
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Group 1
One hundred and sixty healthy infants between 1 and 24 months of age will be evaluated. Subjects will be recruited so that there are 40 subjects within each of four subgroups: 1) Negative ETS exposure and Negative Fm Asthma, 2) Positive ETS exposure and Negative Fm Asthma, 3) Negative ETS exposure and Positive Fm Asthma and 4) Positive ETS exposure and Positive Fm Asthma. Equal numbers of males and females will be recruited. The ethnic composition will be approximately 80% Caucasian and 20% African-American in each of the four groups, which represents the distribution within the cities where infants will be evaluated. Subjects will be excluded if they were born prematurely (\<37 weeks gestation), have a history of congenital cardio-respiratory disease, or have history of lower respiratory illness.
No interventions assigned to this group
Group 2
Eighty infants between 1 and 24 months of age scheduled for CT scans of the abdomen or chest will be evaluated. Subjects will be excluded if they are born prematurely (\<37 weeks gestation), have history of congenital cardio-respiratory disease, or have history of recurrent wheezing.
No interventions assigned to this group
Group 3
Eighty infants with recurrent wheezing between 1 and 24 months of age will be evaluated when they are not acutely symptomatic for at least 3 weeks. Subjects will be recruited so that there are 20 subjects within each of four subgroups: 1) Negative ETS exposure and Negative Fm Asthma, 2) Positive ETS exposure and Negative Fm Asthma, 3) Negative ETS exposure and Positive Fm Asthma and 4) Positive ETS exposure and Positive Fm Asthma. Equal numbers of males and females will be recruited. Subjects will be excluded if they were born prematurely (\<37 weeks gestation) or have history of congenital cardio -respiratory disease.
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
a) Full term \>37 weeks
* Group 2
a) Must have a CT scan nonrespiratory related
* Group 3 a) Must have had at lease 3 episodes of wheezing
Exclusion Criteria
1. cardio-respiratory disease
2. history of recurrent wheezing or lower respiratory infections
* Group 3 a) cardio-respiratory disease
2 Months
2 Years
ALL
No
Sponsors
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National Institutes of Health (NIH)
NIH
Indiana University School of Medicine
OTHER
Responsible Party
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Indiana University
Principal Investigators
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Robert S. Tepper, MD, PhD
Role: PRINCIPAL_INVESTIGATOR
Indiana University School of Medicine
Locations
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Riley Hospital for Children
Indianapolis, Indiana, United States
Countries
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Other Identifiers
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9909-30
Identifier Type: -
Identifier Source: org_study_id