Clinical Observation on the Application of Guasha Synthetics in Primary Dysmenorrhea

Phase 1

Recruiting

• Conditions: Primary dysmenorrhea

• Registration Number: ITMCTR2100004407
• Lead Sponsor: Guangdong Provincial Hospital of Traditional Chinese Medicine

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 20 February 2023

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: Not specified

Inclusion Criteria

1. Subjects who meet the diagnostic criteria of dysmenorrhea of blood stasis type diagnosed by traditional Chinese medicine;
2. Subjects who were diagnosed as primary dysmenorrhea by western medicine;
3. Subjects aged 18-45 years;
4. Subjects with regular menstruation in the past, with a cycle of 21-35 days; the menstrual period is 5-7 days;
5. Patients with good compliance and cooperation with follow-up during the study period;
6. For the subjects with dysmenorrhea for more than 6 months, the VAS score was more than or equal to 4;
7. Volunteers.

Exclusion Criteria

1. Patients with uterine fibroids, adenomyosis, pelvic inflammatory diseases, pelvic blood stasis syndrome, endometriosis, etc. may cause secondary dysmenorrhea;
2. Patients with drug allergy constitution and allergic to moxa oil;
3. Patients with abnormal liver and kidney function;
4. Subjects who participated in other trials within one month;
5. Lactation, preparation for pregnancy, or pregnant women;
6. Subjects with abnormal coagulation function;
7. Subjects with skin diseases or local skin abnormalities.

Study & Design

• Study Type: Interventional study
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
COX;