Comparative Study Between Behavior Therapy and Behavior Therapy Plus Mirabegron in Sexually Active Men With OAB Symptoms
Primary Purpose
Urinary Bladder, Overactive, Sexual Behavior, Sexual Activity
Status
Completed
Phase
Not Applicable
Locations
Taiwan
Study Type
Interventional
Intervention
Behavior therapy alone
Mirabegron 50 MG Extended Release Oral Tablet
Sponsored by
About this trial
This is an interventional treatment trial for Urinary Bladder, Overactive focused on measuring overactive bladder, mirabegron 50mg
Eligibility Criteria
Inclusion Criteria:
- Sexually active men with OAB ≥ 20 years
- Diagnosed with OAB based on OABSS (OABSS urgency score of ≥2 and sum score of ≥3)
- Patients can sign informed consent and record voiding diary
Exclusion Criteria:
- Concurrent use of PDE5 inhibitor or testosterone therapy during study period
- History of stress urinary incontinence
- Neurologic conditions associated with OAB symptoms
- Evidence of active urinary tract infection or urinary tract stone at screening
- Confirmed or suspected genitourinary tract or pelvic malignancy
- Genitourinary tract operation during the 3-month period prior to baseline
- Postvoid residual urine volume (PVR) ≥ 100 mL
- History of uncontrolled hypertension (systolic >180 mmHg and/or diastolic >110 mmHg)
- History of intolerance to mirabegron
- History of medical conditions or presence of patient factors that, in the judgement of the investigator, would preclude adherence to study protocol
- Patient had received intravesical onabotulinumoxinA treatment within recent 6 months
Sites / Locations
- Chang Gung Memorial Hospital, Chang Gung University College of Medicine
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Experimental
Arm Label
Behavior therapy alone
Behavior therapy plus mirabegron 50mg
Arm Description
Behavior therapy alone
Behavior therapy plus Betmiga prolonged-release tablets (mirabegron) 50mg QDAC PO
Outcomes
Primary Outcome Measures
Change from baseline in OABSS at Week 12
Change from baseline in OABSS (Overactive Bladder Symptom Score) at Week 12 (lower OABSS score represent a better outcome)
Change from baseline in IIEF-5 at Week 12
Change from baseline in IIEF-5 (International Index of Erectile Function) at Week 12 (higher IIEF-5 score represent a better outcome)
Secondary Outcome Measures
Change from baseline in OABSS at Week 4
Change from baseline in OABSS (Overactive Bladder Symptom Score) at Week 12 (lower OABSS score represent a better outcome)
Change from baseline in IIEF-5 at Week 4
Change from baseline in IIEF-5 (International Index of Erectile Function) at Week 12 (higher IIEF-5 score represent a better outcome)
Change from baseline in MSHQ-EjD Short Form score at Week 4
Change from baseline in MSHQ-EjD (Male Sexual Health Questionnaire -Ejaculatory Domain) Short Form score at Week 4 (higher MSHQ-EjD Short Form Q1-Q3 sum scores represent a better outcome; lowerer MSHQ-EjD Short Form Q4 score represent a better outcome)
Change from baseline in MSHQ-EjD Short Form score at Week 12
Change from baseline in MSHQ-EjD (Male Sexual Health Questionnaire -Ejaculatory Domain) Short Form score at Week 12 (higher MSHQ-EjD Short Form Q1-Q3 sum scores represent a better outcome; lower MSHQ-EjD Short Form Q4 score represent a better outcome)
Net change of Frequency episode, nocturia episode, urgency episode, UUI episodes in 3-day voiding diary from baseline to 1 and 3 months after the treatment day
Net change of Frequency episode, nocturia episode, urgency episode, UUI episodes in 3-day voiding diary from baseline to 1 and 3 months after the treatment day (lower episode represent a better outcome)
Net change of Qmax from baseline to 1 and 3 months after the treatment day
Net change of maximum flow rate (Qmax) from baseline to 1 and 3 months after the treatment day (higher Qmax and voided volume represent a better outcome)
Net change of voided volume from baseline to 1 and 3 months after the treatment day
Net change of voided volume from baseline to 1 and 3 months after the treatment day (higher voided volume represent a better outcome)
Net change of PVR volume from baseline to 1 and 3 months after the treatment day
Net change of postvoid residual (PVR) volume from baseline to 1 and 3 months after the treatment day (lower PVR represent a better outcome)
Net change of IPSS from baseline to 1 and 3 months after the treatment day
Net change of IPSS (International prostate symptom score) from baseline to 1 and 3 months after the treatment day (lower IPSS represent a better outcome)
Net change of PPBC score from baseline to 1 and 3 months after the treatment day
Net change of PPBC score (Patient perception of bladder condition) from baseline to 1 and 3 months after the treatment day (lower PPBC represent a better outcome)
Net changes of the GRA
Global response assessment (GRA) of satisfaction by the patient (categorized into -3, -2, -1, 0, 1, 2, 3, indicating markedly worse to markedly improved) at 1 and 3 months after the treatment day. An improvement of GRA by 2 scales is considered effective.
Full Information
NCT ID
NCT04420533
First Posted
June 2, 2020
Last Updated
October 4, 2022
Sponsor
Chang Gung Memorial Hospital
1. Study Identification
Unique Protocol Identification Number
NCT04420533
Brief Title
Comparative Study Between Behavior Therapy and Behavior Therapy Plus Mirabegron in Sexually Active Men With OAB Symptoms
Official Title
Comparative Study Between Behavior Therapy and Behavior Therapy Plus Mirabegron 50mg in Sexually Active Men With Bothersome Overactive Bladder Symptoms - A Multicenter, Randomized Study
Study Type
Interventional
2. Study Status
Record Verification Date
October 2022
Overall Recruitment Status
Completed
Study Start Date
June 5, 2020 (Actual)
Primary Completion Date
May 31, 2022 (Actual)
Study Completion Date
August 31, 2022 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Chang Gung Memorial Hospital
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
The objective of this study is to evaluate and compare the therapeutic effects on OAB symptoms, and sexual functions, in terms of erectile function and ejaculatory function, in sexually active OAB male treated with behavior therapy or behavior therapy plus Mirabegron (50 mg).
Detailed Description
Overactive bladder (OAB) syndrome is a subset of storage-predominant lower urinary tract symptoms (LUTS) and has a significant impact on quality of life. Men with OAB generally experience a reduced quality of life, which may include a negative impact on sexual function. A previous study revealed that OAB is associated with erectile dysfunction (ED; prevalence odds ratio, 1.5; 95% confidence interval, 1.1-2.2) to a level comparable with that of hypertension or diabetes, both of which are known risk factors for ED. Furthermore, men with OAB were nine and seven times more likely to report diminished sexual enjoyment and decreased sexual activity, respectively, due to urinary symptoms than men without urinary symptoms.
Behavior therapies are designed as first- line treatment for the treatment of OAB with or without concomitant medication. Mirabegron, a selective β3 adrenoceptor agonist, is indicated for the treatment of OAB. Earlier research studying the role and distribution of β3-adrenoreceptors revealed that the receptors exert other physiological functions such as lipolysis and are present not only in adipose tissue but also in human gall bladder, colon, prostate, skeletal muscles and corpus cavernosum (CC) smooth muscles. It was found that activation by a selective experimental β3-receptor agonist, BRL 37344, elicited relaxation of human CC smooth muscle via a cGMP-dependent but NO-independent mechanism, leading to observable β3-receptor-mediated vasorelaxant tone of CC. The potential effect of β3-receptor agonism at human CC mediated by highly selective mirabegron in both human CC and rat CC that mirabegron markedly relaxed isolated CC strips by activating β3-adrenoceptors localized in cavernosal smooth muscle cells, independently of the NO-cGMP pathway. Recently, intra-cavernosal injection of mirabegron improved erectile function and neurogenic relaxation of corpus cavernosum in diabetic rats.
These early results have spurred research interest in mirabegron-induced CC relaxation and encouraged further clinical studies observing and evaluating the effect of mirabegron on male sexual function. Researchers at Johns Hopkins University has recently completed recruitment of a phase 1 interventional trial (NCT02916693) that aimed to address the hypothesis that activation of β3-adrenoceptors by mirabegron offers an alternative pharmacologic pathway for the treatment of erectile dysfunction. A preliminary small-scale prospective interventional study including 128 male LUTS patients treated with mirabegron 50 mg, 34 of whom had diagnosis of OAB and were sexually active, showed that mirabegron usage did not improve erectile function, as evaluated by International Index of Erectile Function (IIEF-5 4.9% decrease at 4-week; p = 0.106, and 9.1% decrease at 12-week follow-up; p = 0.077). However, the IIEF-5 was significantly decreased in the higher baseline IIEF-5 (≥17) group (11.7% decrease; p = 0.044), noncoronary artery disease (13.2%; p = 0.007) group and non-DM group (13.9% decrease; p = 0.021) at 12-week follow-up.
The accumulated research output warrants the initiation of a prospective study involving a larger patient cohort to evaluate the effect of mirabegron on male sexual function in addition to alleviate OAB symptoms. The objective of this study is to evaluate and compare the therapeutic effects on OAB symptoms, and sexual functions, in terms of erectile function and ejaculatory function, in sexually active OAB male treated with behavior therapy or behavior therapy plus Mirabegron (50 mg).
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Urinary Bladder, Overactive, Sexual Behavior, Sexual Activity, Behavior Therapy, Sexual Function Disturbances
Keywords
overactive bladder, mirabegron 50mg
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
This is a prospective, multi-center, randomized, open label study in sexually active male OAB patients treated with behavior therapy alone or behavior therapy plus mirabegron 50mg OD in a 1:2 ratio.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
150 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Behavior therapy alone
Arm Type
Active Comparator
Arm Description
Behavior therapy alone
Arm Title
Behavior therapy plus mirabegron 50mg
Arm Type
Experimental
Arm Description
Behavior therapy plus Betmiga prolonged-release tablets (mirabegron) 50mg QDAC PO
Intervention Type
Behavioral
Intervention Name(s)
Behavior therapy alone
Intervention Description
reduction of fluid intake at specific times aimed at reducing urinary frequency when most inconvenient;
moderation of intake of caffeine or alcohol, which may have a diuretic and irritant effect, thereby increasing fluid output and enhancing frequency, urgency and nocturia;
use of relaxed and double-voiding techniques;
urethral milking to prevent post-micturition dribble;
distraction techniques such as penile squeeze, breathing exercises, perineal pressure, and mental tricks to take the mind off the bladder and toilet, to help control storage symptoms;
bladder retraining that encourages men to hold on when they have sensory urgency;
reviewing the medication and optimising the time of administration or substituting drugs for others that have fewer urinary effects (these recommendations apply especially to diuretics);
providing necessary assistance when there is impairment of dexterity, mobility or mental state;
treatment of constipation.
Intervention Type
Drug
Intervention Name(s)
Mirabegron 50 MG Extended Release Oral Tablet
Other Intervention Name(s)
Mirabegron 50 MG
Intervention Description
Betmiga prolonged-release tablets (mirabegron) 50mg QDAC PO
Primary Outcome Measure Information:
Title
Change from baseline in OABSS at Week 12
Description
Change from baseline in OABSS (Overactive Bladder Symptom Score) at Week 12 (lower OABSS score represent a better outcome)
Time Frame
Baseline and Week 12
Title
Change from baseline in IIEF-5 at Week 12
Description
Change from baseline in IIEF-5 (International Index of Erectile Function) at Week 12 (higher IIEF-5 score represent a better outcome)
Time Frame
Baseline and Week 12
Secondary Outcome Measure Information:
Title
Change from baseline in OABSS at Week 4
Description
Change from baseline in OABSS (Overactive Bladder Symptom Score) at Week 12 (lower OABSS score represent a better outcome)
Time Frame
Baseline and Week 4
Title
Change from baseline in IIEF-5 at Week 4
Description
Change from baseline in IIEF-5 (International Index of Erectile Function) at Week 12 (higher IIEF-5 score represent a better outcome)
Time Frame
Baseline and Week 4
Title
Change from baseline in MSHQ-EjD Short Form score at Week 4
Description
Change from baseline in MSHQ-EjD (Male Sexual Health Questionnaire -Ejaculatory Domain) Short Form score at Week 4 (higher MSHQ-EjD Short Form Q1-Q3 sum scores represent a better outcome; lowerer MSHQ-EjD Short Form Q4 score represent a better outcome)
Time Frame
Baseline and Week 4
Title
Change from baseline in MSHQ-EjD Short Form score at Week 12
Description
Change from baseline in MSHQ-EjD (Male Sexual Health Questionnaire -Ejaculatory Domain) Short Form score at Week 12 (higher MSHQ-EjD Short Form Q1-Q3 sum scores represent a better outcome; lower MSHQ-EjD Short Form Q4 score represent a better outcome)
Time Frame
Baseline and Week 12
Title
Net change of Frequency episode, nocturia episode, urgency episode, UUI episodes in 3-day voiding diary from baseline to 1 and 3 months after the treatment day
Description
Net change of Frequency episode, nocturia episode, urgency episode, UUI episodes in 3-day voiding diary from baseline to 1 and 3 months after the treatment day (lower episode represent a better outcome)
Time Frame
Baseline, Week 4 and Week 12
Title
Net change of Qmax from baseline to 1 and 3 months after the treatment day
Description
Net change of maximum flow rate (Qmax) from baseline to 1 and 3 months after the treatment day (higher Qmax and voided volume represent a better outcome)
Time Frame
Baseline, Week 4 and Week 12
Title
Net change of voided volume from baseline to 1 and 3 months after the treatment day
Description
Net change of voided volume from baseline to 1 and 3 months after the treatment day (higher voided volume represent a better outcome)
Time Frame
Baseline, Week 4 and Week 12
Title
Net change of PVR volume from baseline to 1 and 3 months after the treatment day
Description
Net change of postvoid residual (PVR) volume from baseline to 1 and 3 months after the treatment day (lower PVR represent a better outcome)
Time Frame
Baseline, Week 4 and Week 12
Title
Net change of IPSS from baseline to 1 and 3 months after the treatment day
Description
Net change of IPSS (International prostate symptom score) from baseline to 1 and 3 months after the treatment day (lower IPSS represent a better outcome)
Time Frame
Baseline, Week 4 and Week 12
Title
Net change of PPBC score from baseline to 1 and 3 months after the treatment day
Description
Net change of PPBC score (Patient perception of bladder condition) from baseline to 1 and 3 months after the treatment day (lower PPBC represent a better outcome)
Time Frame
Baseline, Week 4 and Week 12
Title
Net changes of the GRA
Description
Global response assessment (GRA) of satisfaction by the patient (categorized into -3, -2, -1, 0, 1, 2, 3, indicating markedly worse to markedly improved) at 1 and 3 months after the treatment day. An improvement of GRA by 2 scales is considered effective.
Time Frame
Baseline, Week 4 and Week 12
10. Eligibility
Sex
Male
Minimum Age & Unit of Time
20 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Sexually active men with OAB ≥ 20 years
Diagnosed with OAB based on OABSS (OABSS urgency score of ≥2 and sum score of ≥3)
Patients can sign informed consent and record voiding diary
Exclusion Criteria:
Concurrent use of PDE5 inhibitor or testosterone therapy during study period
History of stress urinary incontinence
Neurologic conditions associated with OAB symptoms
Evidence of active urinary tract infection or urinary tract stone at screening
Confirmed or suspected genitourinary tract or pelvic malignancy
Genitourinary tract operation during the 3-month period prior to baseline
Postvoid residual urine volume (PVR) ≥ 100 mL
History of uncontrolled hypertension (systolic >180 mmHg and/or diastolic >110 mmHg)
History of intolerance to mirabegron
History of medical conditions or presence of patient factors that, in the judgement of the investigator, would preclude adherence to study protocol
Patient had received intravesical onabotulinumoxinA treatment within recent 6 months
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Tsang-Tang Hsieh, MD
Organizational Affiliation
Institutional Review Board Chang Gung Medical Foundation
Official's Role
Study Chair
Facility Information:
Facility Name
Chang Gung Memorial Hospital, Chang Gung University College of Medicine
City
Kaohsiung
ZIP/Postal Code
833
Country
Taiwan
12. IPD Sharing Statement
Citations:
PubMed Identifier
11857671
Citation
Abrams P, Cardozo L, Fall M, Griffiths D, Rosier P, Ulmsten U, van Kerrebroeck P, Victor A, Wein A; Standardisation Sub-committee of the International Continence Society. The standardisation of terminology of lower urinary tract function: report from the Standardisation Sub-committee of the International Continence Society. Neurourol Urodyn. 2002;21(2):167-78. doi: 10.1002/nau.10052. No abstract available.
Results Reference
background
PubMed Identifier
28967230
Citation
Chuang YC, Liu SP, Lee KS, Liao L, Wang J, Yoo TK, Chu R, Sumarsono B. Prevalence of overactive bladder in China, Taiwan and South Korea: Results from a cross-sectional, population-based study. Low Urin Tract Symptoms. 2019 Jan;11(1):48-55. doi: 10.1111/luts.12193. Epub 2017 Oct 2.
Results Reference
background
PubMed Identifier
19090944
Citation
Irwin DE, Milsom I, Reilly K, Hunskaar S, Kopp Z, Herschorn S, Coyne KS, Kelleher CJ, Artibani W, Abrams P. Overactive bladder is associated with erectile dysfunction and reduced sexual quality of life in men. J Sex Med. 2008 Dec;5(12):2904-10. doi: 10.1111/j.1743-6109.2008.01000.x.
Results Reference
background
PubMed Identifier
21492396
Citation
Coyne KS, Sexton CC, Thompson C, Kopp ZS, Milsom I, Kaplan SA. The impact of OAB on sexual health in men and women: results from EpiLUTS. J Sex Med. 2011 Jun;8(6):1603-15. doi: 10.1111/j.1743-6109.2011.02250.x. Epub 2011 Apr 14.
Results Reference
background
PubMed Identifier
17600372
Citation
Yamaguchi O, Chapple CR. Beta3-adrenoceptors in urinary bladder. Neurourol Urodyn. 2007;26(6):752-6. doi: 10.1002/nau.20420.
Results Reference
background
PubMed Identifier
12707413
Citation
Cirino G, Sorrentino R, di Villa Bianca Rd, Popolo A, Palmieri A, Imbimbo C, Fusco F, Longo N, Tajana G, Ignarro LJ, Mirone V. Involvement of beta 3-adrenergic receptor activation via cyclic GMP- but not NO-dependent mechanisms in human corpus cavernosum function. Proc Natl Acad Sci U S A. 2003 Apr 29;100(9):5531-6. doi: 10.1073/pnas.0931347100. Epub 2003 Apr 21.
Results Reference
background
PubMed Identifier
27124860
Citation
Gur S, Peak T, Yafi FA, Kadowitz PJ, Sikka SC, Hellstrom WJ. Mirabegron causes relaxation of human and rat corpus cavernosum: could it be a potential therapy for erectile dysfunction? BJU Int. 2016 Sep;118(3):464-74. doi: 10.1111/bju.13515. Epub 2016 May 26.
Results Reference
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PubMed Identifier
30978726
Citation
Yilmaz-Oral D, Kaya-Sezginer E, Askin D, Hamurtekin Y, Gur S. Mirabegron, A Selective beta3-Adrenoceptor Agonist Causes an Improvement in Erectile Dysfunction in Diabetic Rats. Exp Clin Endocrinol Diabetes. 2021 Mar;129(4):296-302. doi: 10.1055/a-0869-7493. Epub 2019 Apr 12.
Results Reference
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PubMed Identifier
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Citation
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Results Reference
background
Links:
URL
https://uroweb.org/guideline/treatment-of-non-neurogenic-male-luts/
Description
Management of Non-neurogenic Male LUTS. European Association of Urology, 2019 Guidelines
URL
https://clinicaltrials.gov/ct2/show/NCT02916693?term=NCT02916693&draw=2&rank=1
Description
ClinicalTrials.gov Identifier NCT02916693, Mirabegron For Erectile Dysfunction
Learn more about this trial
Comparative Study Between Behavior Therapy and Behavior Therapy Plus Mirabegron in Sexually Active Men With OAB Symptoms
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