None listed
Conditions
Interventions
Poractant alfa, 120mg delivered by aerosolization of a 50mg/ml suspension in 0.9% normal saline, on two occasions administered 30 minutes before bronchial challenge with methacholine chloride.
Sponsors
Woolcock Institute of Medical Research
Study design
Allocation
Randomised controlled trial
Intervention model
Crossover
Primary purpose
Treatment
Masking
Blinded (masking used)
Eligibility
Sex/Gender
All
Age
0 to No maximum
Healthy volunteers
No
Inclusion criteria
Asthma, defined by previous doctor diagnosis and current symptoms or regular therapyNon-asthmatic controls with no history of asthma or other chronic respiratory disease.
Exclusion criteria
Smokers and subjects who are otherwise unsuitable for bronchial challenge will be excluded.
Outcome results
None listed