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Monitoring Asthma Treatment Using Exhaled Nitric Oxide

Monitoring Asthma Treatment Using Exhaled Nitric Oxide

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00562991
Acronym
NOASTHMA
Enrollment
99
Registered
2007-11-26
Start date
2007-10-01
Completion date
2009-12-31
Last updated
2021-01-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Asthma

Keywords

exhaled NO, asthma, child

Brief summary

Asthma is a chronic inflammatory condition in which the airways develop increased responsiveness to various stimuli such as exposure to an allergen, cold air or exercise. It is characterized by airway hyper-responsiveness, inflammation, increased mucus production, and airway obstruction. Since inflammation is an important feature of asthma, the use of non-invasive tests to measure lung inflammation to monitor asthma are of interest.The purpose of the study is to relate costs associated with healthcare utilization and loss of work and school time to the primary health outcome of cumulative number of symptom-free days. This will enable the researchers to determine whether the costs of monitoring exhaled NO to regular management strategy in recently diagnosed asthma will be offset by reductions in other costs of asthma-related care, and, if not, whether the additional costs are likely to be acceptable in terms of the improvement in health outcomes as measured by the additional number of symptom-free days.

Interventions

DEVICEmeasurement of exhaled NO is used to guide treatment

exhaled NO

Sponsors

Merck Sharp & Dohme LLC
CollaboratorINDUSTRY
Aerocrine AB
CollaboratorINDUSTRY
University Hospital, Antwerp
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
5 Years to 14 Years
Healthy volunteers
No

Inclusion criteria

* Male or female children, aged 6-14 years * A documented history of asthma for a period of at least 6 months * Mild to severe persistent asthma according to GINA guidelines * A documented history of allergic sensitization (positive skin prick test or specific IgE * Subject's guardian/parent should be able to complete a symptom score on behalf of the subject. * Subject's guardian/parent should be able to send a symptom score weekly by sms * Both parents have to give written informed consent to participate in the study

Exclusion criteria

* Received any investigational study medication in the 4 weeks prior to screening Visit * Significant comorbidity such as concurrent infection, history of prematurity, history of bronchopulmonary dysplasia, cystic fibrosis, other chronic lung diseases, and other severe chronic diseases * Acute asthma exacerbation within 4 weeks of screening visit * Hospitalization within 12 weeks of screening visit * Systemic corticosteroids within 12 weeks of screening visit * Oral corticosteroid dependence

Design outcomes

Primary

MeasureTime frame
symptom-free days1 year time frame with visits every 3 months

Secondary

MeasureTime frame
days spent in hospital,emergency room visits,physician or nurse contacts use of drugs, days on which school was missed, number of exacerbations1 year time frame

Countries

Belgium

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026