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

Johansson 1998.

Methods Setting: Sweden, primary/secondary care unclear 
 Design: parallel group 
 Length of intervention period: 12 weeks 
 Randomisation: yes, method not stated 
 Allocation concealment: unclear 
 Masking: double blind 
 Excluded: not stated 
 Withdrawals: not stated 
 Baseline characteristics: no demographic data presented 
 Jadad score: 2
Participants 219 subjects 
 Age range: not stated 
 Inclusion criteria: 
 Asthmatic patients symptomatic despite treatment with BDP or BUD 400 mcg/d 
 Exclusion criteria: 
 Not stated
Interventions FP: 200 mcg/d (once daily)
BUD: 400 mcg/d (once daily)
Delivery device: not stated
Outcomes Change in morning PEFR compared to baseline 
 Asthma symptom score 
 Daily use of beta2 agonists
Notes Study in abstract form only
Study also included a treatment arm with FP 100 mcg 2xdaily: results not considered
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 Unclear risk Information not available