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A randomized controlled trial of mirabegran and fesoterodine in overactive bladder

Not Applicable
Conditions
overactive bladder
Registration Number
JPRN-UMIN000038196
Lead Sponsor
Dokkyo Medical University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
150
Inclusion Criteria

Not provided

Exclusion Criteria

patients with a history of hypersensitivity to fesoterodine or mirabegron

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
total score of overactive bladder symptom score
Secondary Outcome Measures
NameTimeMethod
each score of overactive bladder symptom score, total score of overactive bladder symptom score international prostate symptom score, total score of King's Health Questionnaire, frequency volume chart, urofluometry, residual urine
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