Methods | Parallel‐group RCT | |
Participants | Inclusion: grade 2 or 3 cystocele Exclusion: urinary incontinence, previous gynaecological operation, concomitant rectocele or enterocele, recurrent cystocele |
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Interventions | Polypropylene mesh surgery (20 women) vs AC (20 women) | |
Outcomes | Assessed at 6 weeks, 6 months, 1 year Reports the following review outcomes at 1 year:
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Notes | ||
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Low risk | "Allocated by computer programme" |
Allocation concealment (selection bias) | Unclear risk | Method not described |
Blinding of participants and personnel (performance bias) All outcomes | Unclear risk | Blinding not mentioned |
Blinding of outcome assessment (detection bias) All outcomes | Unclear risk | Blinding not mentioned |
Incomplete outcome data (attrition bias) All outcomes | Unclear risk | All 40/40 randomised women were included in analysis |
Selective reporting (reporting bias) | Low risk | Reports main review outcomes |
Other bias | Low risk | Reports "no conflict of interest". No other potential bias identified |