UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000035247
Receipt number R000040161
Scientific Title Efficiency evaluation of coronary computed tomography by using transdermal patch beta-blocker (middle rate)
Date of disclosure of the study information 2018/12/13
Last modified on 2020/06/17 11:44:37

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Basic information

Public title

Efficiency evaluation of coronary computed tomography by using transdermal patch beta-blocker (middle rate)

Acronym

Efficiency evaluation of coronary computed tomography by using transdermal patch beta-blocker (middle rate)

Scientific Title

Efficiency evaluation of coronary computed tomography by using transdermal patch beta-blocker (middle rate)

Scientific Title:Acronym

Efficiency evaluation of coronary computed tomography by using transdermal patch beta-blocker (middle rate)

Region

Japan


Condition

Condition

Ischemic heart disease

Classification by specialty

Medicine in general

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

Efficiency of heart rate reduction by using transdermal patch beta-blocker on coronary computed tomography

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Time until taking an image on coronary computed tomography

Key secondary outcomes

Heart rate reduction on examination day compared to outpatient day


Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit

Individual

Blinding

Open -no one is blinded

Control

No treatment

Stratification


Dynamic allocation


Institution consideration


Blocking

YES

Concealment

Central registration


Intervention

No. of arms

2

Purpose of intervention

Diagnosis

Type of intervention

Medicine

Interventions/Control_1

bisoprolol tape 4mg

Interventions/Control_2

none

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

20 years-old <=

Age-upper limit

100 years-old >

Gender

Male and Female

Key inclusion criteria

Suspicious ischemic heart disease patients

Key exclusion criteria

asthma
chronic kidney disease stage 4.5

Target sample size

60


Research contact person

Name of lead principal investigator

1st name Daisuke
Middle name
Last name Yamazaki

Organization

Tokyo heart center

Division name

Cardiovascular department

Zip code

141-0001

Address

5-4-12 Kita-shinagawa,Shinagawa Tokyo 141-0001, Japan

TEL

0357898100

Email

circulation_777@yahoo.co.jp


Public contact

Name of contact person

1st name Daisuke
Middle name
Last name Yamazaki

Organization

Tokyo heart center

Division name

Cardiovascular department

Zip code

141-0001

Address

5-4-12 Kita-shinagawa,Shinagawa Tokyo 141-0001, Japan

TEL

0357898100

Homepage URL


Email

circulation_777@yahoo.co.jp


Sponsor or person

Institute

Saitama memorial hospital

Institute

Department

Personal name



Funding Source

Organization

none

Organization

Division

Category of Funding Organization

Other

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Saitama memorial hospital

Address

a

Tel

0486863111

Email

yamazaki@tokyoheart.or.jp


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

2018 Year 12 Month 13 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

Open public recruiting

Date of protocol fixation

2018 Year 12 Month 13 Day

Date of IRB

2018 Year 12 Month 10 Day

Anticipated trial start date

2018 Year 12 Month 13 Day

Last follow-up date

2019 Year 10 Month 31 Day

Date of closure to data entry

2019 Year 10 Month 31 Day

Date trial data considered complete

2019 Year 10 Month 31 Day

Date analysis concluded

2019 Year 10 Month 31 Day


Other

Other related information



Management information

Registered date

2018 Year 12 Month 13 Day

Last modified on

2020 Year 06 Month 17 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000040161


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name