Methods | Randomised trial. Method of randomisation not reported | |
Participants | 309 women attending family planning clinics in Beijing, China Included only women attending within 72 h of an unprotected intercourse Excluded women with irregular menstrual periods, who used oral contraceptives and those who had not resumed normal menses after an abortion or delivery |
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Interventions | Mife 25 mg vs Mife 10 mg vs Mife 5 mg | |
Outcomes | Observed number of pregnancies, side effects and changes in menstrual pattern | |
Notes |
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Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Unclear risk | Mentioned randomisation but description not adequate |
Allocation concealment (selection bias) | Unclear risk | Method of allocation concealment not mentioned |
Blinding (performance bias and detection bias) All outcomes | Unclear risk | Not mentioned |
Incomplete outcome data (attrition bias) All outcomes | Low risk | Loss to follow‐up reported |
Selective reporting (reporting bias) | Low risk | Reported planned outcomes |
Other bias | Low risk | None detected |