Loading…

Fifty μg b.i.d. of inhaled fluticasone propionate (FP) are effective in stable asthmatics previously treated with a higher dose of FP

Twenty-seven subjects with moderate asthma at the time of diagnosis, well controlled under regular fluticasone propionate (FP) (250 μg b.i.d.) for 6 months at least, were randomized to receive in double-blind fashion: FP 125 μg b.i.d. (Group 1) or FP 50 μg b.i.d. (Group 2) or placebo (Group 3) for 3...

Full description

Saved in:
Bibliographic Details
Published in:Respiratory medicine 2003-05, Vol.97 (5), p.463-467
Main Authors: GIANNINI, D., DI FRANCO, A., TONELLI, M., BARTOLI, M.L., CARNEVALI, S., CIANCHETTI, S., BACCI, E., DENTE, F.L., VAGAGGINI, B., PAGGIARO, P.L.
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Twenty-seven subjects with moderate asthma at the time of diagnosis, well controlled under regular fluticasone propionate (FP) (250 μg b.i.d.) for 6 months at least, were randomized to receive in double-blind fashion: FP 125 μg b.i.d. (Group 1) or FP 50 μg b.i.d. (Group 2) or placebo (Group 3) for 3 months or until symptom recurrence. Daily symptom score and peak expiratory flow were monitored. At the beginning and at the end of the study, subjects underwent methacholine challenge and sputum induction. Recurrence of symptoms occurred shortly after randomization in all subjects receiving placebo. None from Group 1 or 2 experienced symptom recurrence during the study. No significant difference in clinical and functional data, and in sputum eosinophil percentages was observed between the beginning and the end of the study in both Groups 1 and 2. Subjects from Group 3 showed a significant increase of sputum eosinophils ( P
ISSN:0954-6111
1532-3064
DOI:10.1053/rmed.2002.1458