Methods | Women 'randomly allocated' to 2 groups. A random number table used to generate the allocation sequence and allocation was done by sealed envelopes. Placebos were not used. Side effects were recorded by women | |
Participants | 880 healthy women attending Family Planning Association clinics in Hong Kong Included women with regular menstrual periods (21‐35 days), aged 18‐45 years, with a single act of unprotected intercourse within 48 h of attending the clinic |
|
Interventions | Yuzpe (ethinyl oestradiol 100 μg + norgestrel 1 mg, repeated after 12 h) vs LNG 0.75 mg, orally, 2 doses 12 h apart | |
Outcomes | Observed number of pregnancies, side effects and changes in menstrual pattern | |
Notes |
|
|
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Unclear risk | Women were 'randomly allocated' into 2 groups ‐ doesn't state how |
Allocation concealment (selection bias) | Unclear risk | Method of concealment not stated |
Blinding (performance bias and detection bias) All outcomes | Unclear risk | Blinding not stated |
Incomplete outcome data (attrition bias) All outcomes | Low risk | Reported loss to follow‐up‐ "Of these, 16 subjects in the Yuzpe group and 30 subjects in the levonorgestrel group were lost to follow up after the first visit and the results of treatment were not known. These subjects were excluded from the analysis." |
Selective reporting (reporting bias) | Low risk | Planned outcomes were reported |
Other bias | Low risk | None detected |