IRCT2017061233202N2已完成3 期
Comparison of the effect of Saffron and Fluoxetine in treatment women that have Premenstrual Syndrome
Vice chancellor for research, Sabzevar University of Medical Sciences0 个研究点目标入组 164 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 发起方
- 入组人数
- 164
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 18 years 至 40 years（—）
- 性别
- Female
入选标准
- •informed consent; Eighteen to forty years; regular Menstrual Periods( 35-21 days); Normal cycle (10-3 day); Physical and Mental health; The absence of anemia in the past three months ; Having one or more Symptoms of Premenstrual Syndrome in 2 consecutive cycles; no Pregnancy intention.
- •Exclusion criteria: Underlying disease; Taking other drugs
排除标准
- 未提供
研究者
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