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Treatment of Persistent Wheezing in Infants and Children

Primary Purpose

Asthma, Respiratory Sounds

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Inhaled Fluticasone
Sponsored by
National Heart, Lung, and Blood Institute (NHLBI)
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Asthma focused on measuring Wheezing

Eligibility Criteria

undefined - 36 Months (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Moderate to severe persistent wheezing, as defined by the National Asthma Education and Prevention Program Expert Panel Report 2 No signs of upper or lower respiratory tract infection for at least two weeks prior to study entry Exclusion Criteria: Received therapy with inhaled corticosteroids in the month prior to study entry History of seizures or other neurologic disorders Hypoxemia requiring supplemental oxygen to maintain oxygen saturation above 90% Sepsis Underwent a tracheostomy Heart disease Suspected or documented pulmonary hypertension Currently undergoing assisted ventilation Born at less than 36 weeks gestation

Sites / Locations

  • University of Michigan

Outcomes

Primary Outcome Measures

Change in FEF75 levels
Change in RV/TLC ratio
Loss of bronchodilator responsiveness (measured at the end of the one month treatment period and follow-up evaluation when participant is 5 years of age)

Secondary Outcome Measures

Change in asthma symptom scores (measured at the end of the one month treatment period and follow-up evaluation when participant is 5 years of age)

Full Information

First Posted
March 9, 2006
Last Updated
July 28, 2016
Sponsor
National Heart, Lung, and Blood Institute (NHLBI)
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1. Study Identification

Unique Protocol Identification Number
NCT00301171
Brief Title
Treatment of Persistent Wheezing in Infants and Children
Official Title
Respiratory Function in Infants With Persistent Wheezing
Study Type
Interventional

2. Study Status

Record Verification Date
December 2007
Overall Recruitment Status
Completed
Study Start Date
September 2003 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
August 2007 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
National Heart, Lung, and Blood Institute (NHLBI)

4. Oversight

5. Study Description

Brief Summary
Wheezing is a high-pitched whistling sound that is produced when air flows through narrowed lung airways. It is a common symptom of asthma. Persistent wheezing is commonly treated with bronchodilators and inhaled steroids; however, when wheezing is temporarily caused by a virus or exposure to tobacco smoke, this may not be the most effective treatment. The purpose of this study is to evaluate the cause of wheezing in infants and children and to assess the effectiveness of inhaled steroids on improving lung function.
Detailed Description
Asthma prevalence has steadily increased in the United States since the early 1980s, with infants and young children showing the largest increase. Some young children experience wheezing, but it is not known if this is related specifically to asthma. Wheezing may be caused by a respiratory syncytial virus, maternal smoking, a family history of asthma, or allergies. In addition, some infants who experience wheezing may have small or dysfunctional airways and may not respond well to commonly prescribed anti-inflammatory medications. Because of the many causes of wheezing, in order to prescribe the most effective treatment, it is necessary to thoroughly assess lung function, allergic sensitization, and airway inflammation. The purpose of this study is to examine the causes of moderate to severe wheezing in infants and assess the infants' response to inhaled corticosteroid therapy. The study will also assess new and safer ways to measure lung function and airway inflammation. This study will enroll infants with moderate to severe persistent wheezing. At study entry, participants will undergo lung function testing, which will include a spirometry test, measures of lung volumes, and assessment of bronchodilator responsiveness. Exhaled breath condensate and blood will be collected, and skin-prick testing will be performed to test for allergies. Participants will then be randomly assigned to receive either fluticasone, an inhaled steroid, or placebo for one month. At the end of the month, lung function testing will be performed and exhaled breath and serum measures will be collected to assess airway inflammation. Participants will attend a follow-up evaluation at age 5 years. During the evaluation, lung function, exhaled breath condensate, and serum markers of inflammation will be measured again, and skin-prick testing will also be performed again.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Asthma, Respiratory Sounds
Keywords
Wheezing

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Double
Allocation
Randomized
Enrollment
54 (Anticipated)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Inhaled Fluticasone
Primary Outcome Measure Information:
Title
Change in FEF75 levels
Title
Change in RV/TLC ratio
Title
Loss of bronchodilator responsiveness (measured at the end of the one month treatment period and follow-up evaluation when participant is 5 years of age)
Secondary Outcome Measure Information:
Title
Change in asthma symptom scores (measured at the end of the one month treatment period and follow-up evaluation when participant is 5 years of age)

10. Eligibility

Sex
All
Maximum Age & Unit of Time
36 Months
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Moderate to severe persistent wheezing, as defined by the National Asthma Education and Prevention Program Expert Panel Report 2 No signs of upper or lower respiratory tract infection for at least two weeks prior to study entry Exclusion Criteria: Received therapy with inhaled corticosteroids in the month prior to study entry History of seizures or other neurologic disorders Hypoxemia requiring supplemental oxygen to maintain oxygen saturation above 90% Sepsis Underwent a tracheostomy Heart disease Suspected or documented pulmonary hypertension Currently undergoing assisted ventilation Born at less than 36 weeks gestation
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Amy G. Filbrun, MD
Organizational Affiliation
University of Michigan
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Michigan
City
Ann Arbor
State/Province
Michigan
ZIP/Postal Code
48109
Country
United States

12. IPD Sharing Statement

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Treatment of Persistent Wheezing in Infants and Children

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