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| Name | Class |
|---|---|
| AstraZeneca | INDUSTRY |
| Cystic Fibrosis Foundation | OTHER |
Background Chronic airway inflammation is present in cystic fibrosis. Non-invasive inflammometry may be useful in disease management.
Objective We studied 1) the ability of fractional exhaled nitric oxide and inflammatory markers (acidity, nitrite, nitrate, hydrogen peroxide, 8-isoprostane, interferon-γ, tumor necrosis factor-α, interleukin-2,-4,-5,-10) in exhaled breath condensate, to discriminate between cystic fibrosis and control children, and, 2) the relationship of biomarkers with control and severity of cystic fibrosis.
Methods In 98 children (48 cystic fibrosis / 50 controls), condensate was collected using a glass condenser. Exhaled nitric oxide was measured using the NIOX®.
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Inclusion Criteria:
CF population
Control population
Exclusion Criteria:
For both study populations:
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| Name | Affiliation | Role |
|---|---|---|
| Charlotte M Robroeks, M | Maastricht University Medical Center | Principal Investigator |
| Edward Dompeling, MD, PhD | Maastricht University Medical Center | Study Director |
| Quirijn Jöbsis, MD, PhD | Maastricht University Medical Center | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Catharina Hospital | Eindhoven | Netherlands | ||||
| University Hospital Maastricht |
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| ID | Term |
|---|---|
| D003550 | Cystic Fibrosis |
| ID | Term |
|---|---|
| D010182 | Pancreatic Diseases |
| D004066 | Digestive System Diseases |
| D008171 | Lung Diseases |
| D012140 | Respiratory Tract Diseases |
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| Maastricht |
| 6202AZ |
| Netherlands |
| St Radboud Childrens Hospital | Nijmegen | Netherlands |
| Máxima Medical Centre | Veldhoven | Netherlands |
| D030342 |
| Genetic Diseases, Inborn |
| D009358 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| D007232 | Infant, Newborn, Diseases |