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Multicenter clinical study on magnetic stimulation for female patients with Overactive bladder

Multicenter clinical study on magnetic stimulation for female patients with Overactive bladder

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000031970
Enrollment
Unknown
Registered
2020-04-16
Start date
2020-09-01
Completion date
Unknown
Last updated
2020-06-08

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

Conditions

Female patients with Overactive bladder

Interventions

control group:Tolterodine 2mg, qd
experimental group:Magnetic stimulation therapy

Sponsors

The Second Affiliated Hospital of Zhejiang Chinese Medicine University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
25 Years to 50 Years

Inclusion criteria

Inclusion criteria: 1. Women aged 25-50 years; 2. Patients with negative urine culture and oabss score of 3-11 (mild to moderate), including 2 for urgency of urination and 1 for urgency of incontinence; 3. Patients with a course of more than 3 months; 4. Patients who had not used any drugs for OAB within 3 months before inclusion; 5. Patients who can cooperate with treatment and follow-up.

Exclusion criteria

Exclusion criteria: 1. Patients during pregnancy or preparing for pregnancy; 2. Patients with pelvic organ prolapse; 3. Patients with stress urinary incontinence or mixed urinary incontinence mainly with stress urinary incontinence; 4. Patients with acute and chronic Gynecology, urinary infection, interstitial cystitis, bladder stone, malignant tumor, urethral outlet obstruction, etc.; 5. Patients with a history of transurethral and pelvic surgery; 6. Patients in epilepsy stage; 7. Patients in the acute stage of bleeding at the stimulation site; 8. Patients with implanted metal or electronic instruments near the stimulation site; 9. Patients with serious heart disease or arrhythmia; 10. Patients with urinary retention, myasthenia gravis, ulcerative colitis, and narrow angle glaucoma * 11. Patients with polyuria and severe hepatorenal diseases; 12. Patients with mental and neurological disorders.

Design outcomes

Primary

MeasureTime frame
24-hour urine pad test;24-hour urination diary;OABSS score;ICIQ-OAB;OAB-Q;Urodynamics;

Countries

China

Contacts

Public ContactQing Hu

The Second Affiliated Hospital of Zhejiang Chinese Medicine University

louxiao8@163.com+86 15158053197

Outcome results

None listed

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