primary dysmenorrhea
Conditions
Interventions
Experimental group:Transcutaneous Electrical Acupoint Stimulation(TEAS)
control group:Percutaneous neuromuscular electrical stimulation(TENS)
Sponsors
The Second Affiliated Hospital of Soochow University
Eligibility
Sex/Gender
Female
Age
13 Years to 28 Years
Inclusion criteria
Inclusion criteria: 1. Adolescent childless women meeting the diagnostic criteria for primary dysmenorrhea; 2. Basic regularity of menstruation, no other relevant treatment received in recent three months; 3. No previous history of abdominal surgery, uterine cavity operation, medical abortion, etc.; 4. No cold symptoms and normal temperature in the past two weeks.
Exclusion criteria
Exclusion criteria: 1. Women during pregnancy; 2. Received related treatment for dysmenorrhea in recent three months; 3. Those who have taken painkillers within 24 hours before intervention; 4. Patients with secondary dysmenorrhea (with organic lesions in gynecology); 5. Considering other suspected diseases in combination with medical history, physical examination and auxiliary examinations; 6. Patients with cardiovascular and cerebrovascular diseases, liver, kidney, hematopoietic systems and other primary diseases seriously endangering life, as well as neurological and psychiatric patients.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| VAS-P;Uterine arterial blood flow;Infrared thermal imaging;COX Symptom Inventory score; | — |
Countries
China
Contacts
Public ContactWeipei Zhu
The Second Affiliated Hospital of Soochow University
Outcome results
None listed