Biron‐Shental 2004.
Methods | Randomised trial. | |
Participants | Term, singleton pregnancy BS 4 or less, medical indication for labour induction. | |
Interventions | PGE 2 gel 2 mg (27). Double balloon catheter (26) combined (24) |
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Outcomes | Change in BS, need for oxytocin augmentation. | |
Notes | Outcomes of interest not reported. Setting: Israel Study period: not reported Funding: not reported Declarations of interest: not reported |
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Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Low risk | Computer‐generated sequence. |
Allocation concealment (selection bias) | Unclear risk | Not mentioned. |
Blinding of participants and personnel (performance bias) All outcomes | Unclear risk | Not feasible due to nature of intervention |
Blinding of outcome assessment (detection bias) All outcomes | Unclear risk | Not described |
Incomplete outcome data (attrition bias) All outcomes | Unclear risk | Brief communication, for the reported data no missing. Incomplete outcome data not further mentioned in this report. |
Selective reporting (reporting bias) | Unclear risk | Our outcomes of interest are not reported here, main outcome is change in BS. |
Other bias | Unclear risk | Hard to say, very short report, our outcomes of interest not mentioned, not clear how sample size was calculated. |