Actively Recruiting

Phase Not Applicable
Age: 40Years - 75Years
FEMALE
NCT05635669

Optimized Acupuncture Treatment for Female Stress Urinary Incontinence

Led by Yin Ping · Updated on 2025-05-22

360

Participants Needed

1

Research Sites

203 weeks

Total Duration

On this page

Sponsors

Y

Yin Ping

Lead Sponsor

L

Longhua Hospital

Collaborating Sponsor

AI-Summary

What this Trial Is About

This multicenter randomized controlled trial is designed to explore a relatively suitable application of acupoint combinations and to provide certain clinical evidence for the optimization of acupuncture treatment of female SUI.

CONDITIONS

Official Title

Optimized Acupuncture Treatment for Female Stress Urinary Incontinence

Who Can Participate

Age: 40Years - 75Years
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients with mild to moderate stress urinary incontinence
  • Age between 40 and 75 years
  • Signed informed consent
Not Eligible

You will not qualify if you...

  • Other types of urinary incontinence (urgent, overflow, or mixed)
  • History of urinary incontinence surgery or pelvic floor surgery
  • Pelvic organ prolapse stage II or higher
  • Symptomatic urinary tract infection
  • Residual urine volume greater than 30 mL
  • Maximum urinary flow rate less than 20 mL per second
  • Movement limitations affecting walking, running, or climbing stairs
  • Use of drugs affecting bladder function or receiving specialized SUI treatment
  • Severe cardiovascular, cerebral, liver, kidney, hematopoietic diseases, mental disorders, diabetes, multiple system atrophy, cauda equina neuropathy, or spinal cord disease
  • Pregnancy or breastfeeding
  • Presence of cardiac pacemaker, acupuncture phobia, or metal allergies

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Longhua Hospital Shanghai University of Traditional Chinese Medicine

Shanghai, China

Actively Recruiting

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Research Team

P

PING YIN

CONTACT

Y

YUELAI CHEN

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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