About this trial
To evaluate the efficacy and safety of Honghua Xiaoyao tablets in the treatment of premenstrual syndrome, and the results were further analyzed and evaluated by target trial simulation (TTE) framework.
Eligibility criteria
Qualifiers
Age:18-40 years old (both ends included);
According to the 8th edition of "Obstetrics and Gynecology" (2014), patients diagnosed with premenstrual syndrome;
In accordance with the TCM syndrome differentiation standard of liver depression and qi stagnation.
Disqualifiers
those who were allergic to the ingredients and excipients of Honghua Xiaoyao tablet (exposure group);
In the non-exposed group, those receiving or planning to receive other targeted medications for PMS, such as serotonin reuptake inhibitors (SSRIs), hormones, etc.;
irregular menstrual cycle (menstrual cycle not within 28±7 days);
serious diseases of cardiovascular, cerebrovascular, hematopoietic system, liver and kidney, and malignant tumors;
Trial design
Treatments tested in this trial
- Honghua Xiaoyao tablets
Treatment groups
Locations
Sponsors and collaborators
Lianxin Wang
Lead sponsor
China Academy of Chinese Medical Sciences
Sponsor institution
Chaoyangmen Community Health Service Center of Dongcheng District in Beijing
Collaborator
Hepingli Community Health Service Center,Dongcheng District,Beijing
Collaborator