UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000053344
Receipt number R000060886
Scientific Title Establishment of novel imaging conditions in cardiac MRI: A normal volunteer study on novel imaging conditions in cardiac MRI
Date of disclosure of the study information 2024/01/13
Last modified on 2024/01/13 18:52:27

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Basic information

Public title

Establishment of novel imaging conditions in cardiac MRI: A normal volunteer study on novel imaging conditions in cardiac MRI

Acronym

Studies on novel imaging in cardiac MRI.

Scientific Title

Establishment of novel imaging conditions in cardiac MRI: A normal volunteer study on novel imaging conditions in cardiac MRI

Scientific Title:Acronym

Studies on novel imaging in cardiac MRI.

Region

Japan


Condition

Condition

Cardiovascular disease

Classification by specialty

Radiology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To obtain normal values for multiparametric mapping, MR spectroscopy, elastography, non-contrast angiography, 2D and 4D-flow analysis by simple imaging using our cardiac MRI.

Basic objectives2

Others

Basic objectives -Others

none

Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Normal value

Key secondary outcomes



Base

Study type

Others,meta-analysis etc


Study design

Basic design


Randomization


Randomization unit


Blinding


Control


Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms


Purpose of intervention


Type of intervention


Interventions/Control_1


Interventions/Control_2


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

18 years-old <=

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

(1) Age 18 years or older at the time of obtaining consent.
(2) Able to undergo MRI imaging (not claustrophobic, not after magnetic implantation)
(3) No history of cardiac disease
(4) Patients who have consented to participate in this study.

Key exclusion criteria

(i) History of cardiac disease.
(ii) Claustrophobia, magnetic implantation (pacemaker, prosthesis, implanted metal, coloured contacts).

Target sample size

20


Research contact person

Name of lead principal investigator

1st name Kenji
Middle name
Last name Fukushima

Organization

Fukushima Medical University

Division name

Department of Radiology and Nuclear Medicine

Zip code

960-1295

Address

Hikariga-oka 1, Fukushima city, Fukushima

TEL

0245471334

Email

kfukush4@me.com


Public contact

Name of contact person

1st name Kenji
Middle name
Last name Fukushima

Organization

Fukushima Medical University

Division name

Department of Radiology and Nuclear Medicine

Zip code

960-1295

Address

Hikariga-oka 1, Fukushima city, Fukushima

TEL

0245471334

Homepage URL


Email

kfukush4@fmu.ac.jp


Sponsor or person

Institute

Fukushima Medical University

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

Fukushima Medical University

Address

Hikariga-oka 1, Fukushima city, Fukushima

Tel

0245471334

Email

fmurec@fmu.ac.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

2024 Year 01 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

Preinitiation

Date of protocol fixation

2023 Year 07 Month 01 Day

Date of IRB

2023 Year 06 Month 27 Day

Anticipated trial start date

2024 Year 01 Month 15 Day

Last follow-up date

2024 Year 12 Month 01 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

none


Management information

Registered date

2024 Year 01 Month 13 Day

Last modified on

2024 Year 01 Month 13 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000060886