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 |