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Acupuncture for stress urinary incontinence in menopause women: a randomize controlled study

Not Applicable
Recruiting
Conditions
Stress urinary incontinence
Registration Number
ITMCTR2000003427
Lead Sponsor
The Second Affiliated Hospital of Guangzhou University of Chinese Medicine (Guangdong Provincal hospital of Chinese Medicine)
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Female
Target Recruitment
Not specified
Inclusion Criteria

1. Patients who meet the diagnostic criteria of stress urinary incontinence: according to the recommendation of the Fourth International urinary incontinence Advisory Committee (icud) on female urinary incontinence (4th Edition 2009): I symptoms: laughing, coughing, sneezing and other levels of abdominal pressure increase, urine does not leak out spontaneously; urine flow stops at random when the pressure action stops; II Physical signs: when increasing abdominal pressure, it can be observed that urine leaks out of the urethra involuntarily (pressure induced test) or the positive weight gain of 1H urine pad test is more than 1G; III there is no accompanying symptoms of frequent urination and urgency of urination.
2. Patients aged 40-60 years;
3. Patients with mild to moderate Sui: using ingelman sundberg scale. Mild: urinary incontinence occurs when coughing and sneezing, and no need to use a urinary pad; moderate: urinary incontinence occurs when running, jumping, walking and other daily activities, and it needs to use a urinary pad; severe: urinary incontinence occurs when slight activities and horizontal position changes.
4. Patients who signed informed consent and participated in the study voluntarily.

Exclusion Criteria

1. Patients with urgent urinary incontinence, mixed urinary incontinence and overflowing urinary incontinence (with the assistance of urologist);
2. Patients with previous history of urinary incontinence surgery or pelvic floor surgery;
3. Patients with genital prolapse more than 2 degrees;
4. Patients with symptomatic urinary tract infection;
5. Patients with lower urinary tract obstruction (with the assistance of urologists);
6. Patients with residual urine more than 30 ml;
7. Patients whose maximum flow rate is less than 20 ml / S;
8. Those who can't walk, go upstairs or downstairs, run or have limited activities;
9. Those who have been using drugs that may affect bladder function or who are receiving special treatment for stress urinary incontinence;
10. Patients with severe heart, brain, liver, kidney, hematopoietic system and mental disease, and patients with diabetes, multiple system atrophy, cauda equina neuropathy and myelopathy;
11. Pregnancy or lactation; or the patients who have fertility requirements in the past three months and are not contraception;
12. Objects with pacemaker, metal allergy or serious needle binding;
13. Patients with damaged skin disease and local infection of cheek;
14. Patients with trigeminal neuralgia and facial spasm;
15. Patients with thrombocytopenia and bleeding tendency;
16. Patients with a history of cheek plastic surgery.

Study & Design

Study Type
Interventional study
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
1h urine pad test;The change of 24h urinary incontinence frequency based on 72h micturition diary card;
Secondary Outcome Measures
NameTimeMethod
incontinence impact questionnaire short form;
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