Cooper 1985.
Methods | RCT. Parallel design. Duration: unspecified. Single centre. Country: Canada. |
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Participants | 18 participants with CF and an exacerbation and P. aeruginosa infection. Intervention 1: 10 participants. Intervention 2: 8 participants. |
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Interventions | Intervention 1: IV tobramycin and IV ticarcillin (dose and regimen unstated). Intervention 2: inhaled tobramycin and inhaled carbenicillin (dose and regimen unstated). |
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Outcomes | Lung function (FEV1, FVC % predicted). | |
Notes | We shall seek to contact the authors for IPD to include in any meta‐analysis. Currently SDs for the mean changes observed are not available. | |
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Unclear risk | Described as randomly allocated but no detail given. |
Allocation concealment (selection bias) | Unclear risk | No detail given. |
Blinding of participants and personnel (performance bias) All outcomes | Unclear risk | No detail given. |
Blinding of outcome assessment (detection bias) All outcomes | Unclear risk | No detail given. |
Incomplete outcome data (attrition bias) All outcomes | Unclear risk | 2 participants in each group needed additional antibiotics. Unclear if this was analysed as ITT. |
Selective reporting (reporting bias) | Unclear risk | Insufficient evidence. |
Other bias | Low risk | None identified. |