Primary dysmenorrhea
Conditions
Interventions
Treatment group:Floating needle pre intervention
Waiting for the backup group:Maintain original lifestyle habits without intervention
Sponsors
Shandong Provincial Third Hospital
Eligibility
Sex/Gender
Female
Age
18 Years to 30 Years
Inclusion criteria
Inclusion criteria: (1) Women aged 18 to 30 who have not given birth; (2) Conforming to PD diagnostic criteria: spasmodic pain in the lower abdomen that occurs before or during menstruation without other diseases such as endometriosis; (3) The basic pattern of the cycle is (28 ± 7) d; (4) The visual analogue scale (VAS) score for pain in at least three consecutive menstrual cycles is = 40mm.
Exclusion criteria
Exclusion criteria: (1) Have a history of clinically related serious cardiovascular diseases, liver and kidney dysfunction, and mental illness; (2) Received other related primary dysmenorrhea treatments one month before enrollment; (3) Participating in other clinical trials; (4) Unable to complete or comply with the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Response rate to VAS score decrease in dysmenorrhea after treatment (3rd menstrual cycle) (proportion of patients with VAS score decrease of 50% or VAS score decrease of = 3 points); | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Response rate of dysmenorrhea relief during menstrual cycles 1,2, 4, 5, and 6;VAS score at peak pain intensity per cycle;Duration of dysmenorrhea per cycle (cumulative, degree, h);COX Menstrual Symptom Scale (CMSS);Beck Anxiety Scale, Beck Depression Scale;The demand for painkillers;Patient self-evaluation;Adverse event occurrence rate; | — |
Countries
China
Contacts
Public ContactTianyu Bai
Shandong Provincial Third Hospital
Outcome results
None listed