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The efficacy of PTNS in the treatment of refractory POAB

Percutaneous Tibial Nerve Stimulation for refractory overactive bladder in pediatrics

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600124215
Enrollment
Unknown
Registered
2026-05-08
Start date
2024-08-13
Completion date
Unknown
Last updated
2026-05-11

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

Conditions

refractory overactive bladder in pediatrics

Interventions

test group(PTNS group):Percutaneous Tibial Nerve Stimulation
control group(Solifenacin group):Solifenacin
test group(PTNS combined with Solifenacin group):Percutaneous Tibial Nerve Stimulation combined with Solifenacin Succinate Tablets

Sponsors

The Second Affiliated Hospital of Wenzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
5 Years to 18 Years

Inclusion criteria

Inclusion criteria: 1. Meet the diagnostic criteria for overactive bladder in children: (1) Urgency often accompanied by frequency, nocturia, enuresis, etc., with or without urge urinary incontinence; (2) Exclusion of urinary tract infection or definite pathological factors; 2. Meet the diagnostic criteria for refractory OAB: symptoms such as urgency and urinary incontinence persist after 12 weeks of medication treatment. 3. Age 5 to 18 years old (including 5 and 18 years old), any gender; 4. The child and their guardians voluntarily participate in this trial and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1.Exclude urinary frequency, urgency, and incontinence due to urinary tract infection, spinal cord injury, epilepsy, cerebral insufficiency, diabetes mellitus, and other neurological, urological, and endocrinological disorders. 2.Exclude the ontraindications to the use of solenacin, such as urinary retention , closed-angle glaucoma with uncontrolled symptoms, myasthenia gravis, severe ulcerative colitis, and toxic megacolon. 3.Allergy to the drug or some of the ingredients used in the test was excluded. 4.Patients who have participated or are participating in another clinical trial within 1 month. 5.Patients judged by the investigator to be unsuitable for participation in the clinical trial.

Design outcomes

Primary

MeasureTime frame
Total effective ratio;

Countries

China

Contacts

Public ContactYang Jianhuan

The Second Affiliated Hospital of Wenzhou Medical University

315517813@qq.com+86 135 6622 8082

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 16, 2026