ITMCTR2000004159招募中4 期
A multi-center real-world clinical research program for the application of Motherwort injection in the field of family planning after the market
He'nan Provincial People's Hospital0 个研究点开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 4 期
- 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
- Observational study
入排标准
- 年龄范围
- 18 至 40（—）
- 性别
- Female
入选标准
- •1. After induced abortion
- •Women of childbearing age who were diagnosed with pregnancy and required abortion were selected as the subjects of the study. And meet the following criteria:
- •1) Women eligible for induced abortion;
- •2) Aged18-40 years old, in good health in the past;
- •3) Can fill in the bleeding card;
- •4) Volunteer for the study.
- •(2) After placing the IUD
- •Women of childbearing age who were selected for IUD placement were studied. And meet the following criteria:
- •1) If the IUD is selected and placed as a long-term contraceptive method, or vaginal bleeding >=8 days after the PLACEMENT of the IUD;
- •2) Can fill in the bleeding card;
- •3) Volunteer to participate in the study and sign the informed consent.
- •(3) After the IUD is removed
- •Healthy women who had their IUDs removed were selected and studied for reasons such as pregnancy or menopause. And meet the following criteria:
- •1) Patients aged between 20 and 65 who voluntarily take the ring without surgical contraindications;
- •2) Can fill in the bleeding card;
- •3) Volunteer to participate in the study and sign the informed consent.
排除标准
- •1) Allergy to this product or excipients listed in motherwort preparation and ingredients or history of serious adverse reactions;
- •2) Patients with allergic constitution (allergic to motherwort or to motherwort preparation) + pregnant women;
- •3) Patients whom the researcher considers inappropriate.
研究者
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