Corrigendum to “A dose‐ranging study to determine the efficacy and safety of 1, 2, and 4 mg of dienogest daily for endometriosis” [International Journal of Gynecology and Obstetrics 108 (2010) 21–25]
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This corrigendum clarifies that analyses were based on the full-analysis set, adjusting Fig. 2 for missing rAFS scores and detailing histologic findings for endometriosis in the 2-mg and 4-mg dienogest groups.
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Abstract
The authors wish to clarify that analyses in the paper are based on the full-analysis set (FAS), excluding patients for whom data were unavailable. For the revised American Fertility Society (rAFS) score, data were unavailable in 9.5% of patients in the 2-mg group group at 24 weeks. The columns in Fig. 2 are adjusted to 100%, after excluding these missing data. Histologic examination at 24 weeks in the 2-mg and 4-mg groups identified endometriosis in 33.3% and 46.7%, and no endometriosis in 28.6% and 30.0% of women, with data unavailable in 38.1% and 23.3%, respectively.
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Cited by (3)
- Oral contraceptives in the prevention of endometrioma recurrence: does the different progestins used make a difference? 2013
- Efficacy and safety of Elagolix in the treatment of endometriosis associated pain: a systematic review and network meta-analysis 2021
- New developments in oral contraception: clinical utility of estradiol valerate/dienogest (Natazia®) for contraception and for treatment of heavy menstrual bleeding: patient considerations 2012
Cited by (3)
- Efficacy and safety of Elagolix in the treatment of endometriosis associated pain: a systematic review and network meta-analysis 2021
- Oral contraceptives in the prevention of endometrioma recurrence: does the different progestins used make a difference? 2013
- New developments in oral contraception: clinical utility of estradiol valerate/dienogest (Natazia®) for contraception and for treatment of heavy menstrual bleeding: patient considerations 2012
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