← Back to Clinical Trials
Recruiting Phase 4 NCT06479720

NCT06479720 Efficacy of Solifenacin or Mirabegron With Local Estrogen Versus Combination Pharmacotherapy for Overactive Bladder

◆ AI Clinical Summary
Plain-language summary for patients
Clinical Trial Summary
NCT ID NCT06479720
Status Recruiting
Phase Phase 4
Sponsor Mackay Memorial Hospital
Condition Effect of Drug
Study Type INTERVENTIONAL
Enrollment 300 participants
Start Date 2022-06-16
Primary Completion 2026-06-30

Trial Parameters

Condition Effect of Drug
Sponsor Mackay Memorial Hospital
Study Type INTERVENTIONAL
Phase Phase 4
Enrollment 300
Sex FEMALE
Min Age 40 Years
Max Age 90 Years
Start Date 2022-06-16
Completion 2026-06-30
Interventions
Combined pharmacotherapy with Solifenacin and MirabegronSolifenacin with vaginal estrogen creamMirabegron with vaginal estrogen cream

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

Brief Summary

To investigates the effects of solifenacin or mirabegron with local estrogen versus combination treatment with solifenacin and mirabegron in women with overactive bladder

Eligibility Criteria

Inclusion Criteria: * Patients with detrusor overactivity which defined as a urodynamic observation characterized by involuntary detrusor contractions during the filling phase. Those who were refractory to monotherapy with anti-muscarinics were enrolled for prospective study. Exclusion Criteria: * Postvoid urine retention before treatment * Women who had medical illness and contraindication for using solifenacin and mirabegron, such as narrow-angle glaucoma and hypertension * Concerns for using estrogen include: Women with history of cerebrovascular disease; thromboembolic disorders; gallbladder disease; known or suspected breast carcinoma; estrogen-dependent neoplasm or undiagnosed abnormal genital bleeding.

Related Trials

ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology