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The predictive value of a single dose of beclomethasone.

The predictive value of the acute effect of beclomethasone on a mannitol challenge test for the outcome of longterm treatment with beclomethasone.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON24820
Enrollment
20
Registered
2010-03-30
Start date
2010-05-01
Completion date
Unknown
Last updated
2024-02-28

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

Conditions

asthma bronchial hyperresponsiveness exercise induced asthma

Interventions

A single shot (200µg) of beclomethasone and 4 weeks of treatment with beclomethasone, 200µg twice daily.

Sponsors

Medisch Spectrum Twente, Enschede, the Netherlands
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Age between 12-18 years; 2. Clinical history of allergic asthma and exercise induced bronchoconstriction; 3. Ability to perform reproducible lung function tests (predicted value variation in 3 of 5 consecutive measurements 70% of predicted value.

Exclusion criteria

Exclusion criteria: 1. Other pulmonary or cardiac illnesses; 2. Maximal FEV1 < 70% of predicted value; 3. Use of nasal or systemic corticosteroids, antihistamines, cromoglycates, anticholinergics or leukotriene antagonists in two weeks prior to or during the study; 4. Use of long acting bronchodilator agents 24 hours before testing; 5. Use of short acting bronchodilator agents 8 hours before testing; 6. Hospitalization due to asthma exacerbation in past month; 7. Other changes in asthma medication during treatment period; 8. Upper or lower respiratory tract infections during treatment period; 9. Deviation of the FEV1 before the subsequent mannitol challenges of more than 12 % from baseline FEV1.

Design outcomes

Primary

MeasureTime frame
The correlation between the effect of a single dose of beclomethasone on a mannitol challenge and the effect of 4 weeks of treatment on a mannitol challenge.

Secondary

MeasureTime frame
There will be tested for confounders for this correlation, such as age, gender and baseline lungfunction.

Contacts

Public ContactE.T.G. Kersten

Postbus 50.000

E.Kersten@ziekenhuis-mst.nl+31 (0)53 4872310

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)