dysmenorrhea
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: (1)Meet the diagnostic criteria for primary dysmenorrhea and are experiencing acute attacks of dysmenorrhea; (2)Age 14-35 years; (3)Visual analog score (VAS) >= 4; (4)Have not been treated with acupuncture and taken analgesic medication; (5)Voluntarily participated in this study and signed the informed consent, family informed consent is required for those under 18 years of age. Note: Patients who meet the above 5 items at the same time may be included in this study.
Exclusion criteria
Exclusion criteria: (1) Patients with combined severe life-threatening primary diseases and other acute abdominal pain; (2) Those with severe anxiety, depression, insomnia, and other psychiatric disorders; (3) Women who are pregnant or preparing for pregnancy; (4) Those who are afraid of acupuncture, uncooperate with treatment, or prone to acupuncture fainting. (5) Those who are participating in other clinical trials. (Note: Those who meet the criteria for any one of the above items will be excluded)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Analgesic efficiency at 10 minutes; | — |
Secondary
| Measure | Time frame |
|---|---|
| Analgesic efficiency at0-1?2, 4, 6, 8min time points;Visual Analog Score(VAS);Blind evaluation;Evaluation of compliance; | — |
Countries
China
Contacts
Yunnan University of Chinese Medicine/ The Second Affiliated Hospital of Yunnan University of Traditional Chinese Medicine