Primary dysmenorrhea
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Diagnosed as primary dysmenorrhea according to the primary dysmenorrhea management guidelines issued by the Society of Obstetricians and Gynecologists of Canadian in 2017; 2. Females aged 18 to 30 years who have not given birth; 3. Menstrual cycle regularity: 28±7 days; 4. Periodic pain during menstruation for 6 months and above; 5. The average pain score of the Visual Analogue Scale (VAS) of the last 3 menstrual cycles is >=4 points; 6. Volunteer to participate in the trial and sign an informed consent form.
Exclusion criteria
Exclusion criteria: 1. Patients with secondary dysmenorrhea caused by gynecological diseases such as endometriosis, pelvic inflammatory disease, adenomyosis or other diseases confirmed by gynecological examination and B-ultrasound; 2. Oral contraceptives or drugs that act on the central nervous system within 1 month before treatment, or have received relevant physical therapy; 3. Are participating in or have participated in other drugs or other types of clinical trials within the past 1 month; 4. There are abnormalities such as ulceration and infection in the skin of the irradiation site; 5. Suffering from severe mental or other diseases, unable to correctly score the pain or unable to objectively describe the symptoms; 6. History of phototherapy allergy; 7. Women who are pregnant, breastfeeding or planning to become pregnant; 8. There are objections to the treatment of this trial or the inability to receive regular follow-ups.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| visual analogue scale; | — |
Secondary
| Measure | Time frame |
|---|---|
| Self-rating anxiety scale;Epoxidase dysmenorrhea symptom scale score;Self-rating depression scale;Time and degree of lower abdomen pain; | — |
Countries
China
Contacts
Nanjing Drum Tower Hospital The Affiliated Hospital Of Nanjing University Medical School