ITMCTR2100004761招募中未知
A randomized controlled trial of effectiveness and safety of acupuncture versus transcutaneouse electrical acupoint stimulation on subclinical premature ovarian insufficiency
the Third Affiliated Hospital of Zhejiang Chinese Medical University0 个研究点开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 招募中
- 发起方
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
- 25 至 40（—）
- 性别
- Female
入选标准
- •1. Female patients aged between 25-40 years;
- •2. Havent received any other treatments in the last two months before enrollment;
- •3. Patients voluntarily participate in the study;
- •4. Sign the informed consent form.
排除标准
- •1. Those who are pregnant or have a pregnancy plan in six months;
- •2. Patients with primary amenorrhea;
- •3. Congenital reproductive organ abnormalities;
- •4. Patients with internal diseases which can affect reproductive hormones, such as thyroid disease, SLE, etc.;
- •5. Patients with other serious internal diseases and mental diseases;
- •6. Patients with unilateral or bilateral oophorectomy;
- •7. Those who are unable to tolerate the tests or treatments during the course of this study;
- •8. Those who are participating in other clinical trials.
研究者
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