UMIN-ICDS Clinical Trial

Unique ID issued by UMIN UMIN000050870
Receipt number R000057974
Scientific Title Hemodynamic study of the portal venous region using 3D cine phase contrast MRI (4D Flow MRI)
Date of disclosure of the study information 2023/05/15
Last modified on 2024/04/17 16:43:13

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Basic information

Public title

Hemodynamic study of the portal venous region using 3D cine phase contrast MRI (4D Flow MRI)

Acronym

Hemodynamic study of the portal venous region using 3D cine phase contrast MRI (4D Flow MRI)

Scientific Title

Hemodynamic study of the portal venous region using 3D cine phase contrast MRI (4D Flow MRI)

Scientific Title:Acronym

Hemodynamic study of the portal venous region using 3D cine phase contrast MRI (4D Flow MRI)

Region

Japan


Condition

Condition

abnormal portal venous hemodynamics

Classification by specialty

Hepato-biliary-pancreatic medicine Hepato-biliary-pancreatic surgery Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

We will objectively and quantitatively show how the degree of hepatic injury or transcatheter or surgical intervention in the portal venous region affects portal vein blood flow using blood flow parameters derived from 4D Flow MRI, and clarify the relationship between portal venous blood flow and hepatic regeneration, portal vein thrombus, and treatment efficacy. We will also clarify whether predicting the degree of liver regeneration, the appearance of portal vein thrombi, and the efficacy of interventional and surgical treatment in advance is possible.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1

Confirmatory

Trial characteristics_2

Explanatory

Developmental phase

Not applicable


Assessment

Primary outcomes

For liver transplant donors and recipients, liver volume increase at 3 months postoperatively (increased portal venous blood flow/wall shear stress postoperatively as an exposure/predictor); for cases of portal vein thrombus (RRT value of the main trunk of the portal vein as an exposure/predictor); and for hepatic encephalopathy, improvement of hepatic encephalopathy after transcatheter portal collateral embolization (increased liver blood flow and changes in blood flow from the superior mesenteric vein into the portal vein due to portosystemic shunt embolization as exposure/predictor) will be evaluated.

Key secondary outcomes



Base

Study type

Observational


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

100 years-old >

Gender

Male and Female

Key inclusion criteria

Patients requiring evaluation of blood flow in the portal venous region. Specifically, patients with hepatic dysfunction or patients who require evaluation before and after treatment.
Adult patients who understand the study and have given written consent.

Key exclusion criteria

Patients who have difficulty with MRI imaging, such as claustrophobia or implantation of non-MRI compatible metal devices.
For contrast studies, patients with contrast allergy or renal insufficiency.

Target sample size

250


Research contact person

Name of lead principal investigator

1st name Ryota
Middle name
Last name Hyodo

Organization

Nagoya University Hospital

Division name

Radiology

Zip code

4668560

Address

65, Tsurumai-tyo, Showa-Ku, Nagoya-city, Aichi-ken

TEL

0527442327

Email

ryouta771@med.nagoya-u.ac.jp


Public contact

Name of contact person

1st name Ryota
Middle name
Last name Hyodo

Organization

Nagoya University Hospital

Division name

Radiology

Zip code

4668560

Address

65, Tsurumai-tyo, Showa-Ku, Nagoya-city, Aichi-ken

TEL

0527442327

Homepage URL


Email

ryouta771@med.nagoya-u.ac.jp


Sponsor or person

Institute

Nagoya University

Institute

Department

Personal name

Ryota Hyodo


Funding Source

Organization

Ministry of Education, Culture, Sports, Science and Technology

Organization

Division

Category of Funding Organization

Japanese Governmental office

Nationality of Funding Organization

Japan


Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Nagoya University Hospital

Address

65, Tsurumai-tyo, Showa-Ku, Nagoya-city, Aichi-ken

Tel

0527442423

Email

ethics@med.nagoya-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

名古屋大学医学部附属病院(愛知県)


Other administrative information

Date of disclosure of the study information

2023 Year 05 Month 15 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

2023 Year 05 Month 30 Day

Date of IRB

2023 Year 07 Month 06 Day

Anticipated trial start date

2023 Year 07 Month 06 Day

Last follow-up date

2028 Year 03 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

none


Management information

Registered date

2023 Year 04 Month 17 Day

Last modified on

2024 Year 04 Month 17 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/icdr_e/ctr_view.cgi?recptno=R000057974


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name