Trial record 18 of 755 for:    cystic fibrosis

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

This study has been withdrawn prior to enrollment.
(No problems with planned study- insufficient funding for this study to proceed.)
Information provided by:
Tufts Medical Center Identifier:
First received: September 14, 2009
Last updated: March 17, 2015
Last verified: March 2015

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.

Condition Intervention
Cystic Fibrosis
Procedure: Throat Swab

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Prospective
Official Title: Microbiota of the Respiratory Flora in Children With Cystic Fibrosis During the First Year of Life

Resource links provided by NLM:

Further study details as provided by Tufts Medical Center:

Primary Outcome Measures:
  • To characterize the microbial ecology and changes in bacterial diversity of the oropharynx in a cohort of children with CF during the first year of life using 16S rRNA sequence analysis [ Time Frame: 6-8 weeks of age, 3 months, 6 months, 9 months, and 12 months of age ] [ Designated as safety issue: No ]
  • To describe the clinical variables that may be associated with changes in microbial ecology in children with cystic fibrosis over the first year of life [ Time Frame: 6-8 weeks of age, 3 months, 6 months, 9 months, and 12 months of age ] [ Designated as safety issue: No ]
  • To explore changes in the microbial ecology of the oropharynx in conjunction with Staphylococcus aureus colonization in children with CF [ Time Frame: 6-8 weeks of age, 3 months, 6 months, 9 months, and 12 months of age ] [ Designated as safety issue: No ]

Enrollment: 0
Study Start Date: May 2011
Groups/Cohorts Assigned Interventions
Throat Swab
Infants who have been diagnosed with cystic fibrosis
Procedure: Throat Swab
Swabs will be moistened in sterile 0.9% sodium chloride solution and rotated in the throat and processed for bacterial cultures and for bacterial DNA extraction.


Ages Eligible for Study:   up to 3 Months
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population

Infants with cystic fibrosis


Inclusion Criteria:

  • Male and female subjects, newborn to age 3 months
  • Have a diagnosis of cystic fibrosis (Diagnosis of CF will be based on either a positive sweat chloride of >60 mEq/L or the identification of two detectable mutations associated with CF
  • Parent/guardian plans to have follow-up care for approximately one year at designated CF clinic
  • Parent/guardian provides informed consent to participate in the study

Exclusion Criteria:

  • Contraindications for obtaining oropharyngeal swabs
  Contacts and Locations
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Please refer to this study by its identifier: NCT00977158

United States, Massachusetts
Children's Hospital Boston
Boston, Massachusetts, United States, 02115
Floating Hospital for Children at Tufts Medical Center
Boston, Massachusetts, United States, 02111
Sponsors and Collaborators
Tufts Medical Center
Principal Investigator: Patricia L Hibberd, MD, PhD Tufts Medical Center
  More Information

No publications provided

Responsible Party: Patricia L. Hibberd, MD, PhD, Tufts Medical Center Identifier: NCT00977158     History of Changes
Other Study ID Numbers: 8851
Study First Received: September 14, 2009
Last Updated: March 17, 2015
Health Authority: United States: Institutional Review Board

Keywords provided by Tufts Medical Center:
Cystic Fibrosis
upper respiratory tract
16S rRNA sequence analysis
Staphylococcus aureus
Pseudomonas aeruginosa
Burkholderia cepacia
Haemophilus influenzae
Streptococcus pneumoniae

Additional relevant MeSH terms:
Cystic Fibrosis
Digestive System Diseases
Genetic Diseases, Inborn
Infant, Newborn, Diseases
Lung Diseases
Pancreatic Diseases
Pathologic Processes
Respiratory Tract Diseases processed this record on April 23, 2015