KCT0001967尚未招募未知
Effect of gyejibongneyong-hwan for treatment of dysmenorrhea of uterine fibroids caused by blood stasis: A double blind, randomized placebo controlled trial
适应症
试验速览
- 阶段
- 未知
- 状态
- 尚未招募
- 入组人数
- 38
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional Study
入排标准
- 年龄范围
- 18(Year) 至 45(Year)（—）
- 性别
- Female
入选标准
- •1.Females between 18 and 45 years of age and diagnosed with Blood stasis syndrome.
- •2.Females diagnosed blood stasis through screening test at gynecology
- •3.Confirmation of uterine myomas by ultrasonography (over 2 cm).
- •4.Provide written informed consent to participate in the study.
- •5.Agree to comply with the study regulations.
排除标准
- •1. Patients with heart disease, liver disease, kidney disease or any psychiatric condition.
- •2. Patients who are unable to communicate or are critically ill.
- •3. Pregnant women.
- •5. Patients who take regular medication, including serotonin, anti-depressants, or other anti-psychiatric drugs.
- •4. Patients with any condition that could influence the study assessment.
研究者
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