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sing impulse oscillometry, multiple-breath nitrogen washout and exhaled nitric oxide together to assess asthma inflammatio

Phase 4
Completed
Conditions
Asthma
Respiratory - Asthma
Registration Number
ACTRN12619000287134
Lead Sponsor
niversity of Otago
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
All
Target Recruitment
40
Inclusion Criteria

Physician-diagnosed asthma requiring a minimum of treatment with regular inhaled corticosteroid.

Exclusion Criteria

Diagnosis of COPD, bronchiectasis, lung cancer.
Other co-morbidity likely to affect study participation.
Current smoker (any cigarette smoking within past two months).
Previous ICU admission for acute asthma.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Change in exhaled nitric oxide measured by exhaled nitric oxide analyser[Change from baseline to 30 min post dosing.]
Secondary Outcome Measures
NameTimeMethod
Change in area of reactance measured by impulse oscillometry.[Change from baseline to 30 min post dosing.];Change in lung clearance index measured by multiple breath nitrogen washout.[Change from baseline to 30 min post dosing.];Change in Scond (index of ventilation heterogeneity in the conducting airways) measured by multiple breath nitrogen washout.[Change from baseline to 30 min post dosing.];Change in Sacin (index of ventilation heterogeneity in the acinar airways) measured by multiple breath nitrogen washout.[Change from baseline to 30 min post dosing.];Change in forced vital capacity measured by spirometry.[Change from baseline to 30 min post dosing.];Change in R5-R20 measured by impulse oscillometry.[Change from baseline to 30 min post dosing.]
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