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Inhaled budesonide for adults with mild-to-moderate asthma: a randomized placebo-controlled, double-blind clinical
A L Fernandes1, S M Faresin, M M Amorim
1Respirology Division, Hospital São Paulo, Escola Paulista de Medicina, Universidade Federal de São Paulo, São Paulo, Brazil. analuisa@pneumo.epm.br
Context:
Budesonide is an inhaled corticosteroid with high topical potency and low systemic activity recommended in the treatment of chronic asthma.
Objective:
This study was conducted to determine the efficacy and safety of inhaled budesonide via a breath-activated, multi-dose, dry-powder inhaler.
Type Of Study:
Multicenter randomized parallel-group, placebo-controlled, double-blind, clinical trial.
Setting:
Multicenter study in the university units.
Participants:
Adult patients with mild-to-moderate asthma that was not controlled using bronchodilator therapy alone.
Procedures:
Comparison of budesonide 400 microg administered twice daily via a breath-activated, multi-dose, dry-powder inhaler with placebo, in 43 adult patients (aged 15 to 78 years) with mild-to-moderate asthma (FEV1 71% of predicted normal) that was not controlled using bronchodilator therapy alone.
Main Measurements:
Efficacy was assessed by pulmonary function tests and asthma symptom control (as perceived by the patients) and the use of rescue medication.
Results:
Budesonide 400 microg (bid) was significantly more effective than placebo in improving morning peak expiratory flow (mean difference: 67.9 l/min; P < 0.005) and FEV1 (mean difference: 0.60 l; P < 0.005) over the 8-week treatment period. Onset of action, assessed by morning peak expiratory flow, occurred within the first two weeks of treatment.
Conclusions:
Budesonide via a breath-activated, multi-dose, dry-powder inhaler results in a rapid onset of asthma control, which is maintained over time and is well tolerated in adults with mild-to-moderate asthma.
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