Cystic Fibrosis
Conditions
Brief summary
This study seeks to provide point-of-care clinical diagnostic systems for the diagnosis of current disease status using saliva as a sample specimen.
Detailed description
The overall hypothesis of this study is that whole saliva and its components, due to its direct anatomic relation to the airways, provides a window on the composition and nature of the disease-specific response in the bronchial, sinus, and nasal airways. By examining proteins created in saliva, we hope to validate that saliva is an important diagnostic tool for for rapid analysis of respiratory status. We further propose that rapid salivary diagnostics will improve patient care in prevalent respiratory diseases with frequent health care utilization and high morbidity, such as asthma, chronic obstructive pulmonary disease (COPD), and cystic fibrosis (CF).
Interventions
None listed
Sponsors
Study design
Eligibility
Inclusion criteria
* 6 or more years of age * confirmed Cystic Fibrosis
Exclusion criteria
* Pregnant
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Salivary Biomarkers | Baseline | Biomarkers of inflammation in saliva |
Countries
United States
Contacts
Boston Children's Hospital