Costantini 1982.
Methods | RCT. Parallel design. Duration: mean duration of 15 days. Single centre. Country: Italy. |
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Participants | 19 participants with CF colonised with P. aeruginosa experiencing an exacerbation over 28 exacerbation episodes. Intervention 1: 7 participants. Intervention 2: 10 participants. Invtervention 3: 11 participants. |
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Interventions | Intervention 1: IV carbenicillin 675 mg/kg/day (mean dosage). Intervention 2: IV sisomicin 10.5 mg/kg/day (mean dosage). Invtervention 3: IV carbenicillin 590 mg/kg/day AND IV sisomicin 10 mg/kg/day (mean dosage). |
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Outcomes | Unvalidated clinical score, microbiology and adverse effects. | |
Notes | We shall seek to contact the authors for IPD to reconcile the UoA issues and quantify unpublished data. | |
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Unclear risk | Described as randomised 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 | No withdrawals described. |
Selective reporting (reporting bias) | Unclear risk | Insufficient information. |
Other bias | High risk | UoA issues ‐ 19 participants contributed 28 treatment episodes. |