This study evaluates the effect of intermittent tiotropium bromide and salbutamol as needed versus intermittent fluticasone propionate and salbutamol as needed, or solely, salbutamol as needed on episode-free days in infants and toddlers with recurrent episodes of wheeze and/or shortness of breath.
Up to 30% of all children suffer from episodic wheeze or shortness of breath, i.e. asthmatic bronchitis, during the first three years of life. The condition is usually induced by viral respiratory infections, and short-acting beta-agonists are recommended as a monotherapy for symptoms unless there are at least four physician-confirmed episodes of wheeze or shortness of breath, or three episodes plus asthma risk factors. There is a current need for new therapeutic agents to treat asthmatic bronchitis in young children. In viral-induced wheeze, increased parasympathetic nerve activity results in increased acetylcholine release from nerve endings. Tiotropium bromide, an inhaled anticholinergic agent, prevents the acetylcholine function and achieves mild bronchodilatation and decrease in mucus secretion from the submucosal glands. The aim of the study is to find out the effect of intermittent tiotropium bromide and salbutamol as needed versus intermittent fluticasone propionate and salbutamol as needed, or solely, salbutamol as needed on episode-free days in infants and toddlers with recurrent episodes of wheeze and/or shortness of breath. Episode-free days are defined as those days during which there are no symptoms of wheeze and/or shortness of breath, no unscheduled medical visits for wheeze and/or shortness of breath, and no use of rescue or supplementary controller medications.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
80
Tiotropium Bromide 2.5 µg/dose inhaled aerosol
Fluticasone Propionate 125 µg/dose inhaled aerosol
Salbutamol 0.1 mg/dose inhaled aerosol
Skin and Allergy Hospital, Helsinki University Hospital, Helsinki, Finland
Helsinki, Finland
Percentage of Episode-Free Days
Effect on the episode-free days defined as the days during which there are no symptoms of wheeze and/or shortness of breath, no unscheduled medical visits for wheeze and/or shortness of breath, and no use of rescue or supplementary controller medications.
Time frame: Up to 48 weeks
Number of Participants With Unscheduled Physician Visits
Effect on the number of unscheduled physician visits for episodes of wheeze and/or shortness of breath.
Time frame: Up to 48 weeks
Percentage of Days Participants Needed Rescue Medication
Effect of the treatment on the need for bronchochilative and/or supplementary controller medication.
Time frame: Up to 48 weeks
Number of Participants With Adverse Events
Occurrence of adverse events in treatment groups.
Time frame: Up to 48 weeks
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