KCT0001737已完成未知
A 12 week, randomized, double-blind and placebo-controlled clinical trial to assess the efficacy and safety of soy isoflavone in postmenopausal women
Dr.Chung's Food0 个研究点目标入组 96 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 96
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
- 45(Year) 至 60(Year)（—）
- 性别
- Female
入选标准
- •?last spontaneous menstrual bleeding>12 month ago, aged 45-60 years
- •?hot flushes continued for at least three month
- •?Kupperman index ranged 20 to 40
- •?Serum follicle-stimulating hormone (FSH) levels >= 40 IU /ml.
- •?BMI ranging between 19.0 to 30 kg/m2
- •?Written informed consent
排除标准
- •? women who have hysterectomy or chemotherapy
- •? women who have abnormal finding such as endometrial proliferation, endometrial cancer and uterine cervical cancer related condition
- •? women who have breast cancer related condition
- •? women who received hormone replacement therapy or selective estrogen receptor modulators (SERMS) within five years of enrollment
- •? women who vaginal bleeding, unknown cause within six month of enrollment
- •? Women who have heart, kidney and thyroid disease
- •? Women who have depression and schizophrenia
- •? women who received hormone replacement therapy or selective estrogen receptor modulators (SERMS) within three month of enrollment
- •? Patient with systolic blood pressure =170 mmHg and diastolic pressure =100 mmHg, or hypertensive person who take diuretics (170/100 mmHg, at the screening)
- •? who had uncontrolled bood glucose (IFG 180 mg/dl mmHg, at the screening)
- •? who had soy allergy
- •? who participated other clinical trial within 3 months prior to this study
- •? who are not considrered to be appropriate to particiapt on this study
研究者
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