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 |
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| 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 |