UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000057750
Receipt number R000065995
Scientific Title Fundamental Study on Reducing Imaging Time Using LIPO-Only DWI in Intracranial Large Vessel Occlusion
Date of disclosure of the study information 2025/05/05
Last modified on 2025/05/01 13:41:29

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Basic information

Public title

Fundamental Study on Reducing Imaging Time Using LIPO-Only DWI in Intracranial Large Vessel Occlusion

Acronym

Fundamental Study on Reducing Imaging Time Using LIPO-Only DWI in Intracranial Large Vessel Occlusion

Scientific Title

Fundamental Study on Reducing Imaging Time Using LIPO-Only DWI in Intracranial Large Vessel Occlusion

Scientific Title:Acronym

Fundamental Study on Reducing Imaging Time Using LIPO-Only DWI in Intracranial Large Vessel Occlusion

Region

Japan


Condition

Condition

Volunteer

Classification by specialty

Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To conduct a basic study on the possibility of reducing imaging time in DWI using water selective excitation (LIPO).

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

The use of LIPO-DWI, which is considered to have a high SNR, is expected to reduce imaging time.

Key secondary outcomes



Base

Study type

Interventional


Study design

Basic design

Single arm

Randomization

Non-randomized

Randomization unit


Blinding

Open -no one is blinded

Control

Uncontrolled

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

1

Purpose of intervention

Prevention

Type of intervention

Device,equipment

Interventions/Control_1

Participation period only during MR imaging, with an imaging time of about 5 minutes.

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

60 years-old >

Gender

Male and Female

Key inclusion criteria

Healthy volunteers over 20 years old

Key exclusion criteria

In case of refusal to participate after explanation, or in case of claustrophobia or body implant

Target sample size

20


Research contact person

Name of lead principal investigator

1st name Koji
Middle name
Last name Kawakami

Organization

St. Marianna University School of Medicine Hospital

Division name

Department of Radiologic al Technology

Zip code

2520324

Address

2-16-1 Sugo, Mae-ku, Kawasaki City, Kanagawa

TEL

09096736956

Email

ko0290@marianna-u.ac.jp


Public contact

Name of contact person

1st name Koji
Middle name
Last name Kawakami

Organization

Department of Radiologic al Technology

Division name

Department of Radiologic al Technology

Zip code

2520324

Address

2-16-1 Sugo, Mae-ku, Kawasaki City, Kanagawa

TEL

09096736956

Homepage URL


Email

ko0290@marianna-u.ac.jp


Sponsor or person

Institute

St. Marianna University School of Medicine Hospital

Institute

Department

Personal name



Funding Source

Organization

St. Marianna University School of Medicine Hospital

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

St. Marianna University School of Medicine Hospital

Address

2-16-1 Sugo, Mae-ku, Kawasaki City, Kanagawa

Tel

044-977-8111

Email

ko0290@marianna-u.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

2025 Year 05 Month 05 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

2025 Year 04 Month 01 Day

Date of IRB


Anticipated trial start date

2025 Year 05 Month 02 Day

Last follow-up date

2025 Year 08 Month 01 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2025 Year 05 Month 01 Day

Last modified on

2025 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=R000065995