Mirabegron, solifenacin, combined therapy, and Botox for women with overactive bladder in Taiwan
Official title: Outcome of Different Treatments of Overactive Bladder in Taiwan
Run by Mackay Medical College · NCT07025642 · Data updated 2026-11-12
This will test whether mirabegron, solifenacin, their combination, or intradetrusor Botox reduce the bladder's mechanical work and change bladder compliance in women with overactive bladder.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 30 Years to 100 Years |
| Sex | Women only |
| Enrollment | 60 (estimated) |
| Sponsor | Mackay Medical College Academic / other |
| Locations | 1 site (New Taipei City) |
| Status | Recruiting |
| Started | July 1, 2025 |
| Main results expected | May 1, 2026 |
| Study ends | December 1, 2026 |
| Registry record updated | June 17, 2025 |
| Trial ID | NCT07025642 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Women with overactive bladder who can undergo urodynamic testing and who do not have diabetes, cerebrovascular disease, or other excluded medical conditions are ideal candidates.
✕Probably not a fit
Patients with diabetes, prior stroke, other excluded comorbidities, men, or those with neurogenic bladder are unlikely to be eligible and may not benefit from the study's findings.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This single-center interventional study in New Taipei City applies pressure-volume analysis (PVA), a thermodynamic method adapted from cardiology, to quantify bladder mechanical work per void and to visualize compliance dynamics. Women with overactive bladder will undergo standardized urodynamic evaluations before and after treatment with mirabegron, solifenacin, combined mirabegron+solifenacin, or intradetrusor botulinum toxin A. The study compares changes in PVA-derived work and compliance metrics across treatments to determine how each therapy affects storage and voiding energetics. Patients with diabetes, prior stroke, or other significant comorbidities are excluded to reduce confounding.
Why it matters
Potential benefit: If successful, this could identify which therapy best lowers bladder mechanical workload and improves storage function, helping clinicians choose treatments that reduce symptoms and protect bladder health.
How similar studies have gone: Existing trials show symptomatic benefit for antimuscarinics, beta-3 agonists, and botulinum toxin, but using pressure-volume thermodynamic analysis to quantify bladder work and compliance is a novel and largely untested approach.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: \- female overactive bladder Exclusion Criteria: * DM, CVA, other medical problems
Where it's running
-
Department of Obstetrics and Gynecology
New Taipei City, Taiwan Recruiting
Study contacts
- Study coordinator: Hui-Hsuan Lau, M.D.
- Email: huihsuan1220@gmail.com
- Phone: +886-975-835928
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.