JPRN-UMIN000005079已完成未知
A randomized double blind, placebo-controlled trial of efficacy and safety of Kamishoyosan in patients with climacteric symptoms - A randomized double blind, placebo-controlled trial of efficacy and safety of Kamishoyosan in patients with climacteric symptoms
Hirosaki University Graduate School of Medicine0 个研究点目标入组 200 人开始时间: 2011年3月1日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 200
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
- 40years-old 至 60years-old（—）
- 性别
- Female
入选标准
- 未提供
排除标准
- •1) Patients with serious gastrointestinal weakness 2) Patients with anorexia, nausea and/or vomiting 3) Patients with psycho-neurologic disease (SDS>=60) 4) Patients with a history of drug allergy or hypersensitivity reaction to Kampo medicine 5) Patients with serious complications (hepatic, renal, cardiac diseases or malignancy tumor) 6) Patients who have been participated in other clinical trial within 4months before enrollment, or will participate in a clinical trial. 7) Patients who are assessed to be inappropriate for study participation by the investigator.
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