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临床试验/JPRN-UMIN000041802
JPRN-UMIN000041802已完成未知

A prospective observational study on menstrual symptoms, HRQoL, and work productivity in patients with primary or secondary dysmenorrhea before, during, and after treatment with LEP or non-LEP in Japan - A prospective observational study on menstrual symptoms, HRQoL, and work productivity in patients with primary or secondary dysmenorrhea before, during, and after treatment with LEP or non-LEP in Japan

Bayer Yakuhin, Ltd.0 个研究点目标入组 495 人开始时间: 2020年9月15日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
入组人数
495

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
16years-old 至 39years-old(—)
性别
All

入选标准

  • 未提供

排除标准

  • Patients who meet any of the exclusion criteria will not be enrolled in this study. 1) Patients who have taken LEP for dysmenorrhea in the last 2 months before enrollment 2) Patients with mental disorders such as depression, severe infectious diseases, or malignant tumors 3) Patients with contraindications for LEP or COC 4) Patients who deemed by the investigators to be unsuitable for inclusion in the study (e.g., patients using hormonal agents other than LEP)

研究者

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