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An open, randomized, controlled clinical trial to evaluate the effects of acupuncture and cupping in the treatment for postmenopausal women with stress urinary incontinence

An open, randomized, controlled clinical trial to evaluate the effects of acupuncture and cupping in the treatment for postmenopausal women with stress urinary incontinence

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100047328
Enrollment
Unknown
Registered
2021-06-12
Start date
2021-07-01
Completion date
Unknown
Last updated
2022-02-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Stress urinary incontinence in postmenopausal women

Interventions

Sponsors

Capital Medical University Affiliated Beijing Shijitan Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
40 Years to 80 Years

Inclusion criteria

Inclusion criteria: 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.

Exclusion criteria

Exclusion criteria: 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.

Design outcomes

Primary

MeasureTime frame
1-hour pad test;

Secondary

MeasureTime frame
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;

Countries

China

Contacts

Public ContactShi Li

Capital Medical University Affiliated Beijing Shijitan Hospital,

shili841007@sina.com+86 13716368298

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026