跳至主要内容
临床试验/ISRCTN44184398
ISRCTN44184398已完成4 期

Effectiveness and safety of Hongjin Xiaojie Capsule versus waiting list for breast pain: a multi-center, randomized controlled trial

Yunnan Yousheng Pharmaceutical Co., Ltd0 个研究点目标入组 298 人开始时间: 2019年8月18日最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
298

研究概览

简要总结

2024 Results article in https://pubmed.ncbi.nlm.nih.gov/39232973/ (added 06/09/2024)

研究设计

研究类型
Interventional

入排标准

性别
Female

入选标准

  • 1. 18 - 55 years old, female, pre- or peri-menopause
  • 2. Meeting the diagnostic criteria of breast pain; including women with breast nodules, the longest diameter of B-ultrasonic solid nodules =2cm or the longest diameter of B-ultrasonic cystic nodules =2 cm
  • 3. The number of days of breast pain for each menstrual cycle is equal or longer than 3 days and visual analog scale (VAS) = 4 points; if treated before, the pain symptom could not relieve for three consecutive menstrual cycles or more
  • 4. Women diagnosed as hysteromyoma according to the diagnostic criteria of hysteromyoma will be included
  • 5. The menstrual cycle and the menstrual period are basically regular, and the menstrual cycle is about 28 ± 7 days

排除标准

  • 1. Women who are preparing for pregnancy or who are pregnant or lactating
  • 2. Patients with allergic constitution, or allergic to the test drug or its components
  • 3. Breast image report and data system (BI-RADS) classification > level 3
  • 4. Patients with breast malignant tumors, inflammatory diseases and other endocrine diseases (such as pituitary tumors)
  • 5. Taking contraceptives during the trial and using hormonal drugs within the first three months of screening
  • 6. Those who have taken Chinese or Western medicines to treat this disease within 1 month before screening or those who participated in other clinical drug trials
  • 7. Patients with severe primary diseases including cardiovascular, cerebrovascular, liver, kidney and hematopoietic system, or patients with mental illness

研究者

发起方
Yunnan Yousheng Pharmaceutical Co., Ltd

相似试验