Primary dysmenorrhea
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. For women who have not had children, 18 years old <= 30 years old; 2. Right handed subjects; 3. Subjects meeting the diagnostic criteria of primary dysmenorrhea; 4. The menstrual cycle was normal (28 ± 7 days); 5. The pain score (VAS) of the last menstrual cycle was more than 4 cm; 6. Subjects who signed informed consent.
Exclusion criteria
Exclusion criteria: 1. Subjects with secondary dysmenorrhea caused by polycystic ovary syndrome, hysteromyomatosis, endometriosis or other factors confirmed by B-ultrasound and gynecological examination; 2. Subjects with MRI contraindications, such as claustrophobia, tattoo, implantation of ferromagnetic metal, etc; 3. Subjects with severe anxiety and depression; 4. Subjects with serious life-threatening primary diseases such as cardiovascular, cerebrovascular, liver, kidney and hematopoietic system; 5. Pregnant, pregnant or lactating women; 6. Subjects who had taken painkillers and sedatives within 2 weeks before treatment; 7. Subjects who are participating in other clinical trials.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Visual Analog Scale (VAS); | — |
Secondary
| Measure | Time frame |
|---|---|
| The COX Menstrual Symptom Scale (CMSS);Pain Catastrophizing Scale (PCS);Self-rating Anxiety Scale (SAS);Self-rating Depression Scale (SDS);The 36-item Short Form Health Survey (SF-36); | — |
Countries
China
Contacts
College of acupuncture and massage, Chengdu University of traditional Chinese Medicine