Primary dysmenorrhea
Conditions
Interventions
Sponsors
Third Affiliated Hospital of Sun Yat-sen University
Eligibility
Sex/Gender
Female
Age
16 Years to 35 Years
Inclusion criteria
Inclusion criteria: 1. Patients anticipated the research and signed the informed consent voluntarily; 2. Female patients (16-35 years-old) were diagnosed with primary dysmenorrhea and VAS score=4; 3. Patients were not included in other trials in the past three months; 4. Patients avoid eating cold and spicy food , keep warm and avoid getting cold during the trial.
Exclusion criteria
Exclusion criteria: 1. Patients diagnosed with secondary dysmenorrhea; 2. Patients with irregular menstrual cycle; 3. Patients suffered from the serious diseases of important organs, including liver and kidney dysfunction, brain organic disease, and mental disease. 4. NSAIDS contraindication; 5. Tissue lesions in the selected acupoint area; 6. Pregnant and lactating women; 7. Patients with osteoporosis, coagulation dysfunction, or pacemaker.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| VAS; | — |
Secondary
| Measure | Time frame |
|---|---|
| Basic Data;PGE2;PGF2a;Sleep Interference Scale;Uncomfortable feeling after trial; | — |
Countries
China
Contacts
Public ContactDezhao Liu
Third Affiliated Hospital of Sun Yat-sen University
Outcome results
None listed