Cohort Study of Honghua Xiaoyao Tablets in the Treatment of Premenstrual Syndrome Based on Target Trial Emulation Framework

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age18-40
SponsorLianxin Wang

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

266 Participants
are divided into 1 treatment group

Locations

This trial has no 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