A multicenter, randomized, placebo-controlled, double-blind, comparative study of dienogest at 1 mg/day in patients with primary and secondary dysmenorrhea
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This study evaluated dienogest at 1 mg/day in patients with primary and secondary dysmenorrhea through a multicenter, randomized, placebo-controlled, double-blind design.
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Cited by (4)
- Evaluating the Efficacy and Safety of 48-Week Low-Dose Dienogest Administration in Patients With Dysmenorrhea Caused by Endometriosis: Protocol for a Randomized, Open-Label, Parallel-Group Trial (Preprint) 2024
- Effects of Dienogest on Breasts of Women of Reproductive Age: A Cohort Study 2022
- Efficacy of Low-Dose Estrogen–Progestins and Progestins in Japanese Women with Dysmenorrhea: A Systematic Review and Network Meta-analysis 2022
- Long‐term use of dienogest for the treatment of primary and secondary dysmenorrhea 2020
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