A randomized controlled study to evaluate the efficacy of tamsulosin monotherapy and it combination with mirabegron on patients with overactive bladder induced by benign prostatic hyperplasia
Not Applicable
- Conditions
- Men with overactive bladder induced by benign prostatic hyperplasia
- Registration Number
- JPRN-UMIN000007269
- Lead Sponsor
- Department of Urologu, Sapporo Medical University School of Medicine
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- Male
- Target Recruitment
- 100
Inclusion Criteria
Not provided
Exclusion Criteria
1. Patients with the real child plan 2. Patients suspected malignant disease 3. Patients with urinary retention 4. Ppatients with severe bladder diverticulum 5. Patients with urethral stricture 6. Patients with previous intrapelvic radiation 7. Patients with urinary tract infection, urinary stone, interstitial cystitis 8. Patients with performing clean intermittent catheterization 9. Patients with severe hepatic disorders, severe renal dysfunction and severe cardiovascular diseases 10.Patients who are judged as unsuitable for the trial by doctors.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method