Primary dysmenorrhea
Conditions
Interventions
Experimental group:Yishen Shugan Tiaoshen Method
Sponsors
The Affiliated Hospital of Shandong University of Traditional Chinese Medicine Lixia District Jinan City Shandong Province
Eligibility
Sex/Gender
Female
Age
18 Years to 40 Years
Inclusion criteria
Inclusion criteria: (1) Female aged between 18~40 years old; (2) Meets the diagnostic standards of Western medicine; (3) meet the diagnostic criteria of traditional Chinese medicine; (4) Voluntarily participate in the study and sign the informed consent form;
Exclusion criteria
Exclusion criteria: (1) Suffering from other reproductive system diseases at the same time; (2) Pregnant and lactating females; (3) Patients with local skin infection ulceration or scarring; (4) Patients with spontaneous bleeding or predisposition or poor coagulation function; (5) Unable to cooperate with treatment or mentally ill; (6) Those who are allergic to moxibustion fumes and those who cannot tolerate acupuncture treatment; (7) Patients with contraindications to MRI;
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| cox menstrual symptom scale, CMSS;visual analogue scale VAS;Regional Homogeneity; | — |
Secondary
| Measure | Time frame |
|---|---|
| Self-Rating Depression Scale, SDS;Self-Rating Anxiety Scale, SAS; | — |
Countries
China
Contacts
Public ContactXiaohua Yu
The Affiliated Hospital of Shandong University of Traditional Chinese Medicine
Outcome results
None listed