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Effects of different frequency pulsed magnetic stimulation on female stress urinary incontinence

Effects of different frequency pulsed magnetic stimulation on female stress urinary incontinence

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400085671
Enrollment
Unknown
Registered
2024-06-14
Start date
2024-06-17
Completion date
Unknown
Last updated
2024-07-08

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

Conditions

Stress urinary incontinence

Interventions

Active stimulation Group 1:PFMT+ PMS
Active stimulation Group 2:PFMT+ PMS
Sham stimulation Group:PFMT+ sham PMS

Sponsors

The Second Affiliated Hospital of Soochow University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
25 Years to 45 Years

Inclusion criteria

Inclusion criteria: 1. Women aged 25-45 years with at least one vaginal delivery (at least 6 months since the last delivery); 2. Stress urinary incontinence was diagnosed by an expert in obstetrics and gynecology. The diagnosis was made according to the "Guidelines for the diagnosis and treatment of female stress urinary incontinence (2017)" formulated by the Pelvic Floor Group of Gynecology, Society of Obstetrics and Gynecology, Chinese Medical Association. (i) The patient complained involuntary urine leakage when the abdominal pressure was increased, such as laughing, coughing, sneezing, or walking, without symptoms of frequent urination, urgency, or urge incontinence. (ii) Positive pressure test or positive 1H-pad test (urine leakage =2g).(iii)The severity of SUI was mild or moderate. The Ingelman-Sundberg indexing method was used. Mild: urinary incontinence occurs when coughing or sneezing, no pad is needed , Moderate: urinary incontinence occurs during daily activities such as running, jumping, and fast walking, requiring the use of urine pads); 3. Voluntarily participate in the trial and sign informed consent.

Exclusion criteria

Exclusion criteria: 1.Pregnancy; 2.Urge incontinence and mixed incontinence; 3.Pelvic organ prolapse POP-Q score II or above; 4.Acute urinary or reproductive system infection or vaginal bleeding; 5.History of pelvic radiation therapy or surgery; 6.Implantation of any metal device or electronic device (such as a pacemaker) in the body; 7.Serious heart, brain, liver, kidney diseases, psychological disorders; 8.History of chronic cough and constipation; 9.Malignancy; 10.Body mass index (BMI) >30 kg/m2; 11.Perimenopausal women; 12.Ultrasound showed post-void residual?50ml.

Design outcomes

Primary

MeasureTime frame
1h-pad test;Modified Oxford grading scale (MOS);

Secondary

MeasureTime frame
Incontinence Quality of Life Questionnaire China version (I-QOL);Incontinence impact questionnaire short form China version (IIQ-7);Pelvic organ prolapsed- urinary incontinence sexual questionnaire-12 China version (PISQ-12);3-day bladder diary;Glazer pelvic floor sEMG;transperineal 3-dimensional ultrasound;

Countries

China

Contacts

Public ContactSiyifan Chen

The Second Affiliated Hospital of Soochow University

chensiyifan@163.com+86 139 1406 7236

Outcome results

None listed

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