stress urinary incontinence
Conditions
Interventions
radiofrequency technology vs biofeedback electrical stimulation:none
Sponsors
Third Affiliated Hospital of Southern Medical University
Eligibility
Sex/Gender
Female
Age
18 Years to 80 Years
Inclusion criteria
Inclusion criteria: 1.Postpartum women; 2.Diagnosis is SUI (according to the results of 1 h urine pad test, the urine leakage amount >=2 g is positive. Lightness: 2 g=50 g.) 3.Participate in clinical trials voluntarily and have signed an informed consent form.
Exclusion criteria
Exclusion criteria: 1. Have a history of surgical treatment of urinary incontinence, and a history of pelvic floor surgery in the past six months; 2. POP-Q staging genital prolapse >= 2 degrees; 3. Acute inflammation of the genitourinary tract; 4. There are metal foreign bodies in the body; 5. Those who have been using drugs that may affect bladder function or are receiving other treatments for stress urinary incontinence; 6. Suffer from malignant tumors, serious heart, brain, kidney and other system and mental neuropsychological diseases; 7. The patient is unable to cooperate with the test because of obstacles in consciousness and communication; 8. Patients considered by the investigator to be unsuitable to participate in this clinical trial.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1 h urine pad test;Dairy of urination; | — |
Secondary
| Measure | Time frame |
|---|---|
| International Consultation on Incontinence questionnaire-short form;female secual function index;Pelvic bottom electrophysiologyindex; | — |
Countries
China
Contacts
Public ContactWang Xuefeng
Third Affiliated Hospital of Southern Medical University
Outcome results
None listed