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. 2007 Oct 17;2007(4):CD002310. doi: 10.1002/14651858.CD002310.pub4

Acun 2005.

Methods Setting: Hospital OPD in Turkey 
 Design: parallel group trial 
 Length of intervention period: 52 weeks 
 Randomisation: yes; method not described 
 Masking: open label 
 Excluded: stated (none) 
 Withdrawals: not stated 
 Baseline characteristics: comparable between groups 
 Jadad score: 1
Participants 100 children: 51M 49F 
 Age range: 4‐11.5 years 
 Inclusion criteria: symptomatic 2 x week; recent diagnosis of moderate persistent asthma; nocturnal symptoms >1 night per week; within 10th‐90th centile
Interventions FP: 125 BID (250mcg/d) 
 BUD: 200 BID (400mcg/d)
Inhaler device: MDI
Outcomes Growth rate
Notes  
Risk of bias
Bias Authors' judgement Support for judgement
Adequate sequence generation? Unclear risk Described as randomised; other information not available
Allocation concealment? Unclear risk Information not available
Blinding? 
 All outcomes High risk Open label study