Cystic Fibrosis Clinical Trial
Official title:
Biomarkers in Exhaled Breath Indicate Presence, Control and Severity of Cystic Fibrosis
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®.
n/a
Allocation: Random Sample, Primary Purpose: Screening, Time Perspective: Cross-Sectional
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