ITMCTR2200005956尚未招募4 期
A multicenter, randomized, double-blind study on the efficacy and safety of Gongxuening capsules in reducing postoperative bleeding after induced abortion
适应症
试验速览
- 阶段
- 4 期
- 状态
- 尚未招募
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
- 20 至 40（—）
- 性别
- Female
入选标准
- •1. 20 years old = age = 40 years old;
- •2. Women with intrauterine pregnancy = 10 weeks and requiring termination of pregnancy without contraindications;
- •3. Regular menstrual cycle in the past half a year, no recent (half a year) history of induced abortion;
- •4. The subjects voluntarily signed the informed consent form.
排除标准
- •1. Those who are allergic to the experimental drugs;
- •2. Subjects with contraindications to induced abortion;
- •3. Those with uterine malformation and large uterine fibroids;
- •4. Those with abnormal coagulation function who are using anticoagulant or hemostatic drugs;
- •5. Other circumstances judged by the investigator to be inappropriate for inclusion.
研究者
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