UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000026394
Receipt number R000030328
Scientific Title Comparison in the efficacy of the two add on therapies with an anticholinergic agent versus a beta3-adrenoceptor agonist for patients with benign prostatic enlargement complicated by overactive bladder after alpha1-blocker administration, A randomized, prospective trial using a urodynamic study
Date of disclosure of the study information 2017/03/10
Last modified on 2020/12/24 16:15:51

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Basic information

Public title

Comparison in the efficacy of the two add on therapies with an anticholinergic agent versus a beta3-adrenoceptor agonist for patients with benign prostatic enlargement complicated by overactive bladder after alpha1-blocker administration, A randomized, prospective trial using a urodynamic study

Acronym

Comparison in the efficacy of the two add on therapies with an anticholinergic agent versus a beta3-adrenoceptor agonist for BPH/OAB

Scientific Title

Comparison in the efficacy of the two add on therapies with an anticholinergic agent versus a beta3-adrenoceptor agonist for patients with benign prostatic enlargement complicated by overactive bladder after alpha1-blocker administration, A randomized, prospective trial using a urodynamic study

Scientific Title:Acronym

Comparison in the efficacy of the two add on therapies with an anticholinergic agent versus a beta3-adrenoceptor agonist for BPH/OAB

Region

Japan


Condition

Condition

benign prostatic enlargement complicated by overactive bladder

Classification by specialty

Urology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To investigate in the efficacy of the two add on therapies with fesoterodine versus a mirabegron for patients with benign prostatic enlargement complicated by overactive bladder after alpah1-blocker administration using a urodynamic study

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1

Exploratory

Trial characteristics_2

Pragmatic

Developmental phase

Phase IV


Assessment

Primary outcomes

the change of storage and voiding function between the two add on therapies after 12 weeks' treatment

Key secondary outcomes

the change of subjective symptoms regarding lower urinary tract symptoms between the two add on therapies after 12 weeks' treatment


Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit

Individual

Blinding

Open -no one is blinded

Control

Active

Stratification

NO

Dynamic allocation

NO

Institution consideration

Institution is not considered as adjustment factor.

Blocking

NO

Concealment

Numbered container method


Intervention

No. of arms

2

Purpose of intervention

Treatment

Type of intervention

Medicine

Interventions/Control_1

The administration of fesoterodine

Interventions/Control_2

The administration of mirabegron

Interventions/Control_3


Interventions/Control_4


Interventions/Control_5


Interventions/Control_6


Interventions/Control_7


Interventions/Control_8


Interventions/Control_9


Interventions/Control_10



Eligibility

Age-lower limit

50 years-old <=

Age-upper limit

90 years-old >=

Gender

Male

Key inclusion criteria

1) patinets who have taken alpha-1 blocker for more than 12 weeks
2) total OAB symptom scores (OABSS) more than 2 and urinary urgency episodes more than 1 per week
3) outpatinets more than 50 years old

Key exclusion criteria

Patients were excluded if they received oral treatment with propafenone hydrochloride, flecainide acetate, anticholinergic agents, antidepressants, anti-anxiety agents, or sex hormonal agents; had neurogenic bladder dysfunction, bladder calculi, or active urinary tract infection; and had severe cardiac disease, renal dysfunction (serum creatinine level more than 2 mg/dL), and hepatic dysfunction (aspartate and alanine aminotransferase concentrations more than twice the normal values).

Target sample size

100


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Yoshihisa Matsukawa

Organization

Nagoya University Graduate School of Medicine

Division name

Department of Urology

Zip code


Address

65 tsurumai, showa-ku, Nagoya, JAPAN

TEL

052-744-2985

Email

yoshi44@med.nagoya-u.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Yoshihisa Matsukawa

Organization

Nagoya University Graduate School of Medicine

Division name

Department of Urology

Zip code


Address

65 tsurumai, showa-ku, Nagoya, JAPAN

TEL

052-744-2985

Homepage URL


Email

yoshi44@med.nagoya-u.ac.jp


Sponsor or person

Institute

Nagoya University Graduate School of Medicine

Institute

Department

Personal name



Funding Source

Organization

none

Organization

Division

Category of Funding Organization

Self funding

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization


Address


Tel


Email



Secondary IDs

Secondary IDs

NO

Study ID_1


Org. issuing International ID_1


Study ID_2


Org. issuing International ID_2


IND to MHLW



Institutions

Institutions



Other administrative information

Date of disclosure of the study information

2017 Year 03 Month 10 Day


Related information

URL releasing protocol


Publication of results

Unpublished


Result

URL related to results and publications


Number of participants that the trial has enrolled


Results


Results date posted


Results Delayed


Results Delay Reason


Date of the first journal publication of results


Baseline Characteristics


Participant flow


Adverse events


Outcome measures


Plan to share IPD


IPD sharing Plan description



Progress

Recruitment status

Completed

Date of protocol fixation

2017 Year 03 Month 08 Day

Date of IRB

2017 Year 06 Month 05 Day

Anticipated trial start date

2017 Year 06 Month 05 Day

Last follow-up date

2018 Year 09 Month 30 Day

Date of closure to data entry

2018 Year 10 Month 20 Day

Date trial data considered complete

2018 Year 10 Month 31 Day

Date analysis concluded

2018 Year 12 Month 31 Day


Other

Other related information



Management information

Registered date

2017 Year 03 Month 04 Day

Last modified on

2020 Year 12 Month 24 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000030328


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name