UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000014468
Receipt number R000016833
Scientific Title Tuning up parameters in newly-developed MRI sequences for neuro and neck imaging
Date of disclosure of the study information 2014/07/07
Last modified on 2015/05/01 11:03:57

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Basic information

Public title

Tuning up parameters in newly-developed MRI sequences for neuro and neck imaging

Acronym

Tuning up parameters in neuro and neck MRI sequences

Scientific Title

Tuning up parameters in newly-developed MRI sequences for neuro and neck imaging

Scientific Title:Acronym

Tuning up parameters in neuro and neck MRI sequences

Region

Japan


Condition

Condition

Healthy young volunteers

Classification by specialty

Radiology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To adjust imaging parameters for newly-developed the neuro and neck MRI sequences.

Basic objectives2

Others

Basic objectives -Others

To evaluate the image quality.

Trial characteristics_1

Exploratory

Trial characteristics_2

Others

Developmental phase

Not applicable


Assessment

Primary outcomes

To find optimized imaging parameters.

Key secondary outcomes

To evaluate the quality of the images acquired using newly-developed sequences.


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

20 years-old <=

Age-upper limit

35 years-old >=

Gender

Male and Female

Key inclusion criteria

Healthy young people

Key exclusion criteria

1. Pregnancy or suggestive of pregnancy
2. Implanted electorical, megnetical or mechanical device in the body
3. Claustrophobia
4. There are non-compliant items in the questionaries.
5. A participant in any other clinical study
6. Person who is ruled unfit to be a participant in this study.

Target sample size

40


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Shigeo Okuda

Organization

Keio University School of Medicine

Division name

Department of Diagnostic Radiology

Zip code


Address

35 Shinanomachi, Shinjyuku-ku, Tokyo

TEL

03-5363-3837

Email

okuda@rad.med.keio.c.jp


Public contact

Name of contact person

1st name
Middle name
Last name Shigeo Okuda

Organization

Keio University School of Medicine

Division name

Department of Diagnostic Radiology

Zip code


Address

35 Shinoanmachi, Shinjyuku-ku, Tokyo, Japan

TEL

03-5363-3837

Homepage URL


Email

okuda@rad.med.keio.ac.jp


Sponsor or person

Institute

Keio University School of Medicine

Institute

Department

Personal name



Funding Source

Organization

GE Healthcare Japan

Organization

Division

Category of Funding Organization

Profit organization

Nationality of Funding Organization

Japan


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

2014 Year 07 Month 07 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

Synthetic DWI and IFIR compressed sensing (CS) were used for brain DWI and MRA of cervical arteries. The synthetic DWI (composed from b= 0, 100, 200, 500, 1000) was equivalent to direct images with b-values of 1500 and 2000. The best parameters for cervical MRA using IFIR-CS was concluded to be ARC of 3x1 and CS of 2.5.

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

2014 Year 05 Month 30 Day

Date of IRB


Anticipated trial start date

2014 Year 07 Month 07 Day

Last follow-up date

2015 Year 06 Month 30 Day

Date of closure to data entry

2015 Year 06 Month 30 Day

Date trial data considered complete

2015 Year 06 Month 30 Day

Date analysis concluded

2015 Year 06 Month 30 Day


Other

Other related information

Acquired images will be evaluated for assessing image quality.


Management information

Registered date

2014 Year 07 Month 03 Day

Last modified on

2015 Year 05 Month 01 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000016833


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name