An open, randomized, controlled clinical trial to evaluate the effects of acupuncture and cupping in the treatment for postmenopausal women with stress urinary incontinence
- Conditions
- Stress urinary incontinence in postmenopausal women
- Registration Number
- ITMCTR2100004942
- Lead Sponsor
- Capital Medical University Affiliated Beijing Shijitan Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- Not specified
1. Conform to the diagnostic criteria of SUI in the Guidelines for the Diagnosis and Treatment of Female Stress Urinary Incontinence (2017);
2. More than 12 months since the woman's last menstruation.
1. 1h urine pad test shows that the leaked urine volume >= 50g;
2. Routine urine examinations suggest urinary tract infection;
3. Have taken drugs for urinary incontinence or that may affect lower urinary tract function, or received non-drug therapy for urinary incontinence (electrical stimulation, bladder training, pelvic floor muscle training, etc.) in the past month;
4. There is a history of surgical treatment for urinary incontinence and history of pelvic floor surgery;
5. Pelvic organ prolapse >= II degree;
6. Suffer from other system diseases that affect lower urethral function, such as uncontrolled diabetes, multiple sclerosis, Parkinson's disease, spinal cord injury, cauda equina injury, multiple system atrophy, etc.;
7. Accompanied by severe heart, lung, liver, kidney and hematopoietic diseases, neurological and mental diseases, and cognitive dysfunction.
Study & Design
- Study Type
- Interventional study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1-hour pad test;
- Secondary Outcome Measures
Name Time Method International Consultation on Incontinence Questionnaire-Short Form;Incontinence quality of life questionnaires;The average number of urinary incontinence within 24 hours;Three-dimensional ultrasound examination of pelvic floor lesions;