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Clinical trial for improving the quality of life of female patients with stress urinary incontinence treated by long needle penetrating

Clinical trial for improving the quality of life of female patients with stress urinary incontinence treated by long needle penetrating

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR1900002400
Enrollment
Unknown
Registered
2019-06-14
Start date
2017-10-01
Completion date
Unknown
Last updated
2023-02-20

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

Conditions

Stress urinary incontinence

Interventions

Experimental group:Zhibian(BL54) penetrating Shuidao(ST28)" method
Control group:Zhongji, Pangguangsu, Shensu, Shanyinjiao

Sponsors

Shanxi University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
32 Years to 69 Years

Inclusion criteria

Inclusion criteria: (1) Female aged 30 to 70 years; (2) Meet the diagnostic standard of stress urinary incontinence; (3) attending this experiment voluntarily.

Exclusion criteria

Exclusion criteria: (1) with other type of urinary incontinence; (2) combing with urine system infection; (3) with the history of Pelvic reconstructive surgery and SUI surgery; (4) combing with diabetes, cauda equine syndrome and spinal cord problems; (5) taking adrenal hormone related medicine; (6) with peacekeeper or sensitive to mental materials; (7) with pregnancy or in nursing period; (8) attending other trials; (9) other reasons.

Design outcomes

Primary

MeasureTime frame
I-QOL;—

Secondary

MeasureTime frame
72h urine diary card;1 hour pad;—

Countries

China

Contacts

Public ContactLaixi Ji

Shanxi University of Chinese Medicine

tyjilaixi@126.com+86 13509714277

Outcome results

None listed

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