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Comparison of Solifenacin and Mirabegron in Treatment of Overactive Bladder Symptoms in Men After TURP

Primary Purpose

Overactive Bladder Syndrome

Status
Unknown status
Phase
Phase 2
Locations
Taiwan
Study Type
Interventional
Intervention
Solifenacin 5Mg
Mirabegron 50 MG
Sponsored by
Buddhist Tzu Chi General Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Overactive Bladder Syndrome focused on measuring Overactive bladder, Transurethral Resection of the Prostate, Pharmacotherapy, Mirabegron, Solifenacin

Eligibility Criteria

20 Years - 80 Years (Adult, Older Adult)MaleDoes not accept healthy volunteers

Inclusion Criteria:

  1. Male patients with BPH and undergo TURP or TUIP.
  2. Patients void smoothly after catheter removal.
  3. No active urinary tract infection.
  4. No gross hematuria or blood clot obstruction.
  5. Patient or his care giver can complete voiding diary and report symptoms.

Exclusion Criteria:

  1. Patients have overt neurological diseases such as cerebrovascular disease, senile dementia or spinal cord injury.
  2. Patients have severe medical disease and completely immobile.
  3. Patients have PVR larger than 150ml.
  4. Patients do not have OAB after TURP.

Sites / Locations

  • Buddhist Tzu Chi General HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

No Intervention

Arm Label

Solifenacin 5 mg for 4 weeks

Mirabegron 50 mg for 4 weeks

Control: non treatment

Arm Description

Solifenacin 5 mg once-daily for 4 weeks.

Mirabegron 50 mg once-daily for 4 weeks.

Control: non treatment.

Outcomes

Primary Outcome Measures

Urgency Severity Scale (USS)
The change of USS from baseline to 4 weeks after catheter removal and starting OAB medication.

Secondary Outcome Measures

Overactive Bladder Symptom Score (OABSS)
The changes of OABSS
frequency episodes, urgency episodes, urgency urinary incontinence (UUI) episodes in the 3-day voiding diary
The changes of frequency episodes, urgency episodes, urgency urinary incontinence (UUI) episodes in the 3-day voiding diary
maximum flow rate (Qmax)
The changes of maximum flow rate (Qmax)
voided volume (Vol)
The changes of voided volume (Vol)
Postvoid residual volume (PVR)
The changes of Postvoid residual volume (PVR)
International Prostate Symptom Score (IPSS)
The changes of International Prostate Symptom Score (IPSS)
quality of life index (QoL-I)
The changes of quality of life index (QoL-I)

Full Information

First Posted
August 13, 2018
Last Updated
August 23, 2018
Sponsor
Buddhist Tzu Chi General Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT03632772
Brief Title
Comparison of Solifenacin and Mirabegron in Treatment of Overactive Bladder Symptoms in Men After TURP
Official Title
Comparative Study of Solifenacin and Mirabegron in Treatment of Overactive Bladder Symptoms in Men After Transurethral Resection of the Prostate - A Randomized Prospective Study
Study Type
Interventional

2. Study Status

Record Verification Date
August 2018
Overall Recruitment Status
Unknown status
Study Start Date
August 1, 2018 (Actual)
Primary Completion Date
July 31, 2019 (Anticipated)
Study Completion Date
July 31, 2019 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Buddhist Tzu Chi General Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Urinary frequency urgency and urgency urinary incontinence (UUI) are commonly encountered in patients after transurethral prostatectomy (TURP) or transurethral incision of the prostate (TUIP). Antimuscarinics has been widely used to treat OAB and around 70% of patients can improve symptoms after treatment. Beta-3 adrenoceptor agonist (mirabegron) can also decrease DO and improve OAB symptoms. Combination treatment of solifenacin 5mg plus mirabegron 25 or 50mg was more effective than mirabegron 50mg alone, but with more anticholinergic side effects. However, there has been no clinical trial to compare which drug provides more benefit to decrease the OAB symptom severity immediately after TURP. This study tries to compare the safety and therapeutic efficacy between solifenacin and mirabegron in men with BPH and having OAB symptoms immediately after TURP. This study was designed as a prospective, randomized trial to compare the safety and efficacy of OAB medication on the decrease of overactive bladder symptoms score (OABSS) and urgency severity score (USS) between solifenacin 5mg QD and mirabegron 50mg QD in men with BPH undergoing TURP. A total of 130 male patients with BPH and undergo TURP or TUIP will be enrolled. The primary end point is the change of USS from baseline to 4 weeks after catheter removal and starting OAB medication. Secondary end-points include the changes of OABSS, frequency episodes, urgency episodes, UUI episodes in the 3-day voiding diary, maximum flow rate (Qmax), voided volume and PVR, International Prostate Symptom Score (IPSS) and quality of life index (QoL-I) from baseline to 2 weeks and 4 weeks. We expect that patients receiving solifenacin and mirabegron might have similar therapeutic effects on decrease of USS, but patients who received mirabegron might have less adverse events such as dry mouth or difficulty in urination.
Detailed Description
Introduction: Urinary frequency urgency and urgency urinary incontinence (UUI) are commonly encountered in patients after transurethral prostatectomy (TURP) or transurethral incision of the prostate (TUIP). [1] Patients usually bother by these overactive bladder (OAB) symptoms. The causes of postprostatectomy OAB might be detrusor overactivity (DO) before TURP, increase afferent input due to acute inflammation after TURP, or a weak urethral sphincter which cannot hold urine at the bladder capacity. Antimuscarinics and beta-3 adrenoceptor agonist are two different classes of medication for OAB. [2] Antimuscarinics has been widely used to treat OAB and around 70% of patients can improve symptoms after treatment. Beta-3 adrenoceptor agonist (mirabegron) can also decrease DO and improve OAB symptoms. Combination treatment of solifenacin 5mg plus mirabegron 25 or 50mg was more effective than mirabegron 50mg alone, but with more anticholinergic side effects. [3] However, antimuscarnics might decrease detrusor contractility and result in increase of postvoid residual (PVR) volume. Current clinical studies reveal that mirabegron does not impair detrusor contractility or increase PVR. [4] Under this consideration, mirabegron has been widely used to treat male lower urinary tract symptoms (LUTS) due to benign prostate hyperplasia (BPH). [5] However, there has been no clinical trial to compare which drug provides more benefit to decrease the OAB symptom severity immediately after TURP. This study tries to compare the safety and therapeutic efficacy between solifenacin and mirabegron in men with BPH and having OAB symptoms immediately after TURP. Material and methods: Objectives and Endpoints: This study was designed as a prospective, randomized trial to compare the safety and efficacy of OAB medication on the decrease of overactive bladder symptoms score (OABSS) and urgency severity score (USS) between solifenacin 5mg QD and mirabegron 50mg QD in men with BPH undergoing TURP. Randomization: Permuted block randomization method will be applied to generate randomization codes. Each randomization number will be assigned to individual patient according to the time-sequence for screened patient become eligible. Expected Results: Patients receiving solifenacin and mirabegron might have similar therapeutic effects on decrease of USS, but patients who received mirabegron might have less adverse events such as dry mouth or difficulty in urination.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Overactive Bladder Syndrome
Keywords
Overactive bladder, Transurethral Resection of the Prostate, Pharmacotherapy, Mirabegron, Solifenacin

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
130 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Solifenacin 5 mg for 4 weeks
Arm Type
Experimental
Arm Description
Solifenacin 5 mg once-daily for 4 weeks.
Arm Title
Mirabegron 50 mg for 4 weeks
Arm Type
Experimental
Arm Description
Mirabegron 50 mg once-daily for 4 weeks.
Arm Title
Control: non treatment
Arm Type
No Intervention
Arm Description
Control: non treatment.
Intervention Type
Drug
Intervention Name(s)
Solifenacin 5Mg
Other Intervention Name(s)
Vesicare
Intervention Description
We compared the safety and therapeutic efficacy between Solifenacin and Mirabegron in men with benign prostate hyperplasia and having overactive bladder symptoms immediately after Transurethral Resection of the Prostate.
Intervention Type
Drug
Intervention Name(s)
Mirabegron 50 MG
Other Intervention Name(s)
Betmiga
Intervention Description
We compared the safety and therapeutic efficacy between Solifenacin and Mirabegron in men with benign prostate hyperplasia and having overactive bladder symptoms immediately after Transurethral Resection of the Prostate.
Primary Outcome Measure Information:
Title
Urgency Severity Scale (USS)
Description
The change of USS from baseline to 4 weeks after catheter removal and starting OAB medication.
Time Frame
from baseline to 4 weeks
Secondary Outcome Measure Information:
Title
Overactive Bladder Symptom Score (OABSS)
Description
The changes of OABSS
Time Frame
from baseline to 2 weeks and 4 weeks.
Title
frequency episodes, urgency episodes, urgency urinary incontinence (UUI) episodes in the 3-day voiding diary
Description
The changes of frequency episodes, urgency episodes, urgency urinary incontinence (UUI) episodes in the 3-day voiding diary
Time Frame
from baseline to 2 weeks and 4 weeks.
Title
maximum flow rate (Qmax)
Description
The changes of maximum flow rate (Qmax)
Time Frame
from baseline to 2 weeks and 4 weeks.
Title
voided volume (Vol)
Description
The changes of voided volume (Vol)
Time Frame
from baseline to 2 weeks and 4 weeks.
Title
Postvoid residual volume (PVR)
Description
The changes of Postvoid residual volume (PVR)
Time Frame
from baseline to 2 weeks and 4 weeks.
Title
International Prostate Symptom Score (IPSS)
Description
The changes of International Prostate Symptom Score (IPSS)
Time Frame
from baseline to 2 weeks and 4 weeks.
Title
quality of life index (QoL-I)
Description
The changes of quality of life index (QoL-I)
Time Frame
from baseline to 2 weeks and 4 weeks.

10. Eligibility

Sex
Male
Gender Based
Yes
Gender Eligibility Description
Male patients with benign prostate hyperplasia (BPH) and undergo transurethral prostatectomy (TURP) or transurethral incision of the prostate (TUIP).
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Male patients with BPH and undergo TURP or TUIP. Patients void smoothly after catheter removal. No active urinary tract infection. No gross hematuria or blood clot obstruction. Patient or his care giver can complete voiding diary and report symptoms. Exclusion Criteria: Patients have overt neurological diseases such as cerebrovascular disease, senile dementia or spinal cord injury. Patients have severe medical disease and completely immobile. Patients have PVR larger than 150ml. Patients do not have OAB after TURP.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Hann-Chorng Kuo, M.D.
Phone
886-3-8561825
Ext
12113
Email
hck@tzuchi.com.tw
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Hann-Chorng Kuo, M.D.
Organizational Affiliation
Department of Urology, Buddhist Tzu Chi General Hospital, Hualien
Official's Role
Principal Investigator
Facility Information:
Facility Name
Buddhist Tzu Chi General Hospital
City
Hualien city
ZIP/Postal Code
970
Country
Taiwan
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Hann-Chorng Kuo, M.D.
Phone
886-3-8561825
Ext
2113
Email
hck@tzuchi.com.tw

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
IPD was not planned to share.
Citations:
PubMed Identifier
18973143
Citation
Seki N, Yuki K, Takei M, Yamaguchi A, Naito S. Analysis of the prognostic factors for overactive bladder symptoms following surgical treatment in patients with benign prostatic obstruction. Neurourol Urodyn. 2009;28(3):197-201. doi: 10.1002/nau.20619.
Results Reference
background
PubMed Identifier
29709423
Citation
Yamada S, Ito Y, Nishijima S, Kadekawa K, Sugaya K. Basic and clinical aspects of antimuscarinic agents used to treat overactive bladder. Pharmacol Ther. 2018 Sep;189:130-148. doi: 10.1016/j.pharmthera.2018.04.010. Epub 2018 Apr 27.
Results Reference
background
PubMed Identifier
29699858
Citation
Kelleher C, Hakimi Z, Zur R, Siddiqui E, Maman K, Aballea S, Nazir J, Chapple C. Efficacy and Tolerability of Mirabegron Compared with Antimuscarinic Monotherapy or Combination Therapies for Overactive Bladder: A Systematic Review and Network Meta-analysis. Eur Urol. 2018 Sep;74(3):324-333. doi: 10.1016/j.eururo.2018.03.020. Epub 2018 Apr 23.
Results Reference
background
PubMed Identifier
27619782
Citation
Wada N, Iuchi H, Kita M, Hashizume K, Matsumoto S, Kakizaki H. Urodynamic Efficacy and Safety of Mirabegron Add-on Treatment with Tamsulosin for Japanese Male Patients with Overactive Bladder. Low Urin Tract Symptoms. 2016 Sep;8(3):171-6. doi: 10.1111/luts.12091. Epub 2015 Feb 17.
Results Reference
background
PubMed Identifier
23727415
Citation
Nitti VW, Rosenberg S, Mitcheson DH, He W, Fakhoury A, Martin NE. Urodynamics and safety of the beta(3)-adrenoceptor agonist mirabegron in males with lower urinary tract symptoms and bladder outlet obstruction. J Urol. 2013 Oct;190(4):1320-7. doi: 10.1016/j.juro.2013.05.062. Epub 2013 May 30.
Results Reference
background

Learn more about this trial

Comparison of Solifenacin and Mirabegron in Treatment of Overactive Bladder Symptoms in Men After TURP

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