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Comparison of therapeutic effects of electroacupuncture at different time interval of treatment on female stress urinary incontinence: a randomized controlled trial

Comparison of therapeutic effects of electroacupuncture at different time interval of treatment on female stress urinary incontinence: a randomized controlled trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-INR-17012762
Enrollment
Unknown
Registered
2017-09-20
Start date
2017-09-21
Completion date
Unknown
Last updated
2017-10-02

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

Conditions

female stress urinary incontinence

Interventions

Sponsors

Guang’anmen Hospital, China Academy of Chinese Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
35 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Meet the 2009 International Consultation on Urological Diseases(ICUD)diagnostic criteria for stress urinary incontinence 2. Female whose age ranged from 35 to 75 years; At the same time, the above 2 items can be included in this study.

Exclusion criteria

Exclusion criteria: 1. Other types of incontinence, such as urgency urinary incontinence, mixed urinary incontinence, bladder excessive filled urinary incontinence; 2. Symptom of frequent micturition or urgent micturition; 3. symptomatic urinary tract infection; 4. History of urinary incontinence or pelvic floor surgery; 5. Prolapse of pelvic organs = 2 degrees; 6. Residual urine > 30ml; 7. Qmax = 20ml/s; 8. Limitation of walking, climbing stairs and running action; 9. Accept other forms of treatment for the disease, such as medication, pelvic floor exercises, transcutaneous electrical nerve stimulation, or the use of other drugs that have an effect on bladder function; 10. Patients with severe heart, brain, liver, kidney, and hematopoietic and psychiatric disorders; 11. Pregnancy or lactation; 12. Patients with a pacemaker; 13. Severely ill looking or allergic to metal; 14. Cognitive impairment, can not understand the content of the scale evaluation. Those who meet any of the above 1 items shall be excluded.

Design outcomes

Primary

MeasureTime frame
Decrease by fifty percent of 24h stress urinary incontinence comparing with baseline during treatment;

Secondary

MeasureTime frame
Decrease by fifty percent of 24h stress urinary incontinence comparing with baseline during follow-up period;Decrease of 24h stress urinary incontinence comparing with baseline;ICIQ-SF;1 hour pad test;1 hour urine pad test, incontinence volume increased by 50% and over the baseline number of patients;The utilization and mean of urine pad varied from baseline;Number and average times of specialist treatment;Expectation value evaluation of Acupuncture;

Countries

China

Contacts

Public ContactZhao Yuwei

Guang’anmen Hospital, China Academy of Chinese Medical Sciences

506113296@qq.com+86 13651060969

Outcome results

None listed

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