Ref (type) | Population | Outcome, Interventions | Results and statistical analysis | Effect size | Favours |
Adverse effects | |||||
RCT |
68 women, aged 25–45 years with regular periods, premenstrual distress for at least 6 months, diagnosis confirmed by prospective daily symptom rating assessment |
Adverse effects
with subcutaneous estradiol implant plus oral norethisterone with placebo implant plus oral placebo |
Significance not reported |