Methods |
Women 'randomly allocated' to 3 groups. Method of randomisation not reported |
Participants |
240 women attending the clinic in an MCH hospital, Henan, China. Women had regular menstrual periods and a single act of unprotected intercourse within 120 h of attending the clinic |
Interventions |
Mife 75 mg vs Mife 50 mg vs Mife 10 mg, orally |
Outcomes |
Observed number of pregnancies, side effects and changes in menstrual pattern |
Notes |
Loss to follow‐up: Mife 75 mg: 2; Mife 50 mg: 3; Mife 10 mg: 6
Observed pregnancy/total number of women: Mife 75 mg: 1/78; Mife 50 mg: 1/77; Mife 10 mg: 1/74
|
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 was reported |
Selective reporting (reporting bias) |
Low risk |
Planned outcome of pregnancy rate was reported |
Other bias |
Low risk |
None detected |