Asthma Clinical Trial
Official title:
A Multicenter, Device Randomized, Open-label Prospective Single-cohort Study of Monitoring Exhaled NO in Symptomatic Asthmatic Adults and Children During Anti-inflammatory Treatment
The purpose of this study is to demonstrate substantial equivalence between two medical devices which measure nitric oxide in exhaled breath, NIOX MINO® and NIOX® in Symptomatic Asthmatic Adults and Children.
Asthma is a chronic inflammatory disorder of the airways. Chronically inflamed airways are
hyperresponsive; they become obstructed and airflow is limited (by bronchoconstriction,
mucus plugs, and increased inflammation) when airways are exposed to various risk factors.
Asthma causes recurring episodes of wheezing, breathlessness, chest tightness, and coughing
particularly at night or in the early morning.
NO is an important endogenous regulatory molecule that is widely distributed throughout the
body. The detection of NO in exhaled air was first reported in 1991, and, soon after it was
shown that the levels NO in exhaled air are elevated in patients with asthma. There is now
much evidence showing that measurement of the concentration of NO in exhaled air offers a
useful non−invasive method of assessing inflammatory airway disease.
Exhaled NO is not increased during bronchospasm unless there is coexisting inflammation.
Exhaled NO may have a valuable role in differentiating between the inflammatory and
bronchospastic components of clinical asthma, and is also useful for guiding the therapeutic
use of steroids and other anti−inflammatory agents.
A study on asthmatics and non−asthmatics subjects has shown that substantial equivalence
exists between the stationary device NIOX® and the hand held device NIOX MINO® when
comparing NO measurements, when similar conditions are considered and examinations are made
as consistently as possible.
In a study with the stationary device NIOX®, exhaled NO was measured before and after two
weeks of inhaled corticosteroid treatment in unstable steroid−naïve adult and paediatric
asthmatic subjects. The result was a 50.5% mean reduction of exhaled NO. The change in
exhaled NO was also compared to change in standard asthma outcome measures, asthma symptoms
and spirometry.
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Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Diagnostic
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