Microbiota of the Respiratory Flora in Children With Cystic Fibrosis During the First Year of Life



Status:Archived
Conditions:Pulmonary
Therapuetic Areas:Pulmonary / Respiratory Diseases
Healthy:No
Age Range:Any
Updated:7/1/2011
Start Date:May 2011

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The goal of this study is characterize the changes in bacterial diversity of the upper
respiratory tracts of infants with cystic fibrosis (CF). Another goal is to determine when
CF patients become colonized with pathogenic bacteria that are responsible for the lethal
lung damage in children with CF. Ten subjects will be recruited into the study. Throat swabs
will be collected at 6-8 weeks of age, 3 months, 6 months, 9 months, and 12 months of age in
order to chart any changes in the bacterial populations of the respiratory tract. Clinical
data will also be collected to evaluate the possible influence of external factors on
changes in the microbial communities. This study will provide preliminary data on whether
probiotics can eradicate the colonization of the respiratory tract by pathogenic bacteria.



We found this trial at
2
sites
300 Longwood Avenue
Boston, Massachusetts 02115
617-355-6000
Children's Hospital - Boston Boston Children's Hospital is a 395-bed comprehensive center for pediatric health...
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Boston, Massachusetts 02111
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Boston, MA
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