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Clinical Trial Summary

To investigates the effects of botulinum toxin type A bladder injection compared to combined pharmacotherapy with Mirabegron and Solifenacin.


Clinical Trial Description

Patients with detrusor overactivity who were refractory to monotherapy with either anti-muscarinics or β3-adrenoceptor agonists were enrolled for prospective study. Patient were divided in two groups, intradetrusor onabotulinumtoxinA injection and combined pharmacotherapy with Mirabegron and Solifenacin. Incontinence-related symptoms distress and impact on quality of life were evaluated by short form of Urinary Distress Inventory, (UDI-6), Incontinence Impact Questionnaire (IIQ-7) and Overactive Bladder Symptom Score (OABSS). Objective outcomes include changes from baseline in daily urgency episodes, urinary incontinence episodes, maximum cystometric capacity, maximum detrusor pressure (Pdetmax) at first involuntary detrusor contraction and volume at first involuntary detrusor contraction were measured. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05968885
Study type Interventional
Source Mackay Memorial Hospital
Contact Hui-Hsuan Lau, MD
Phone +886-2-25433535
Email huihsuan1220@gmail.com
Status Recruiting
Phase Phase 4
Start date October 1, 2021
Completion date June 30, 2025

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