Urinary Incontinence Clinical Trials

Find Urinary Incontinence Clinical Trials Near You

Efficacy and Safety of Solifenacin or Mirabegron With Local Estrogen Versus Combination Treatment With Mirabegron and Solifenacin for Refractory Overactive Bladder

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 4
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
Participation Requirements
Sex: Female
Minimum Age: 40
Maximum Age: 90
Healthy Volunteers: f
View:

• 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.

Locations
Other Locations
Taiwan
Mackay Memorial Hospital
RECRUITING
Taipei
Contact Information
Primary
Hui-Hsuan Lau, MD
huihsuan1220@gmail.com
+886-2-25433535
Time Frame
Start Date: 2022-06-16
Estimated Completion Date: 2026-12-31
Participants
Target number of participants: 300
Treatments
Active_comparator: Solifenacin and mirabegron
Solifenacin 5mg and Mirabegron 25mg
Experimental: Solifenacin with vaginal estrogen cream
Solifenacin 5mg once per day with vaginal conjugated equine estrogen (CEE) 0.625 mg twice a week.
Experimental: Mirabegron with vaginal estrogen cream
Mirabegron 25mg once per day with vaginal conjugated equine estrogen (CEE) 0.625 mg twice a week.
Related Therapeutic Areas
Sponsors
Leads: Mackay Memorial Hospital

This content was sourced from clinicaltrials.gov