primary dysmenorrhea
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1.Those who meet the above diagnostic criteria for PDM; 2.Aged between 18-35 years old; 3. Those with a VAS score of 4 or more; 4. Those who have regular menstrual cycles; 5. Those who have not taken any pain-relieving drugs within 1 month before treatment; 6.Willing to accept abdominal acupuncture treatment and willing to cooperate in completing the relevant procedures of this experiment.
Exclusion criteria
Exclusion criteria: 1.Diagnosis of secondary dysmenorrhea, or the presence of organic pathologies such as pelvic inflammatory disease, endometriosis, uterine fibroids, etc; 2.Combination of serious primary diseases such as liver, kidney, hematopoietic system, cardiovascular system, or mental illness; 3.Concurrently receiving other treatments related to the treatment of this disease; 4.Infection of the skin at the trigger point site and abnormal coagulation function; 5.Others: not treated according to the provisions of this clinical trial, withdrawing halfway, etc
Design outcomes
Secondary
| Measure | Time frame |
|---|---|
| intra-abdominal pressure;Pressure Pain Threshold;two-point discrimination;point-to-point test;two point estimation;Muscle Structure and Morphology;Surface Electromyographic (sEMG) Signals of Abdominal Muscles;Skin Conductance;Skin Temperature;Heart Rate; | — |
Primary
| Measure | Time frame |
|---|---|
| Visual Analogue Scale for Pain;Short-Form McGill Pain Questionnaire , SF-MPQ; | — |
Countries
China
Contacts
Shanghai Yangpu District Central Hospital (Tongji University Affiliated Yangpu Hospital)