ITMCTR2100004709尚未招募1 期
Clinical randomized controlled trial of dingkundan oral liquid in the treatment of primary dysmenorrhea
Xiyuan Hospital, Chinese Academy of Traditional Chinese Medicine0 个研究点开始时间: 待定最近更新:
试验速览
- 阶段
- 1 期
- 状态
- 尚未招募
- 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
- 18 至 30(—)
- 性别
- Female
入选标准
- •1. Patients met the diagnostic criteria of consensus guideline for primary dysmenorrhea of SOGC 2017;
- •2. According to the syndrome differentiation standard of cold coagulation and blood stasis syndrome;
- •3. Patients aged between 18 and 30 years who have not given birth (need contraception during medication);
- •4. The former menstrual cycle was regular (28 ± 7 days);
- •5. Vas (Visual analog pain score)>= 4;
- •6. Voluntary informed consent.
排除标准
- •1. Secondary dysmenorrhea caused by endometriosis, adenomyosis and pelvic inflammatory disease;
- •2. Patients who use intrauterine device and plan pregnancy within 6 months;
- •3. Patients who used long-acting contraceptives by injection or subcutaneous implantation within 6 months, or who took oral contraceptives for less than 8 weeks were in washout period;
- •4. There are serious primary heart, liver, lung, kidney, blood or other serious diseases affecting survival, such as tumor;
- •5. Disabled patients stipulated by law (deaf, dumb, blind, mental retardation, spermatic impairment);
- •6. Suspected or history of drug or alcohol abuse;
- •7. Allergic weight, allergic to two or more drugs or food, or allergic to known components of the drug;
- •8. Patients who are participating in clinical trials of other drugs;
- •9. Patients with other diseases or conditions that reduce the possibility of enrollment or complicate enrollment, such as frequent changes in working environment, unstable living environment, etc., which are likely to cause loss of follow-up.
研究者
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