Methods |
Double‐blind randomised trial. Method of randomisation not reported |
Participants |
120 women attending a family planning clinic in Tianjing, China. Women had regular menstrual periods and attended the clinic within 72 h of a single act of unprotected intercourse |
Interventions |
Mife 10 mg + placebo, 12 h apart vs LNG 0.75 mg, 2 doses, 12 h apart |
Outcomes |
Observed number of pregnancies, side effects and changes in menstrual pattern |
Notes |
Post‐randomisation exclusions or loss to follow‐up not reported
Observed pregnancy/expected pregnancy/total number women: Mife + placebo 0/5/60; LNG 0/5/60
|
Risk of bias |
Bias |
Authors' judgement |
Support for judgement |
Random sequence generation (selection bias) |
Unclear risk |
Method of randomisation not reported |
Allocation concealment (selection bias) |
Unclear risk |
Method of allocation concealment not mentioned |
Blinding (performance bias and detection bias) All outcomes |
Low risk |
Double‐blind |
Incomplete outcome data (attrition bias) All outcomes |
Unclear risk |
Post‐randomisation exclusions or loss to follow‐up not reported |
Selective reporting (reporting bias) |
Low risk |
Reported planned outcomes |
Other bias |
Low risk |
None detected |