UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000018214
Receipt number R000020665
Scientific Title The prospective study on the development prevention prevention of biliary stricture after liver transplantation
Date of disclosure of the study information 2015/07/06
Last modified on 2015/07/06 14:52:18

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Basic information

Public title

The prospective study on the development prevention prevention of biliary stricture after liver transplantation

Acronym

The prospective study on the development prevention prevention of biliary stricture after liver transplantation

Scientific Title

The prospective study on the development prevention prevention of biliary stricture after liver transplantation

Scientific Title:Acronym

The prospective study on the development prevention prevention of biliary stricture after liver transplantation

Region

Japan


Condition

Condition

Living-donor liver transplantation

Classification by specialty

Hepato-biliary-pancreatic surgery

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

Develop the onset prevention prophylaxis of biliary stricture after liver transplantation

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Biliary stricture incidence after liver transplantation

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

Historical

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

1

Purpose of intervention

Prevention

Type of intervention

Device,equipment

Interventions/Control_1

Placed the plastic stent at the
biliary anastomosis

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


Not applicable

Gender

Male and Female

Key inclusion criteria

20 years of age or older of liver transplant recipients in all cases
Men and women No preference

Key exclusion criteria

Patients who have not obtained the consent of the present study

Target sample size

20


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Kazuhisa Takeda

Organization

Yokohama City University Hospital

Division name

Gastroenterological surgery

Zip code


Address

3-9 Fukuura, Kanazawa-ku, Yokohama city, 236-0004 Japan

TEL

045-787-2800

Email

kazutake@yokohama-cu.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Kazuhisa Takeda

Organization

Yokohama city University Hospital

Division name

gastroenterological surgery

Zip code


Address

3-9 Fukuura, Kanazawa-ku, Yokohama City, 236-0004 Japan

TEL

045-787-2800

Homepage URL


Email

kazutake@yokohama-cu.ac.jp


Sponsor or person

Institute

Yokohama city University 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


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

2015 Year 07 Month 06 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

2015 Year 05 Month 01 Day

Date of IRB


Anticipated trial start date

2015 Year 05 Month 01 Day

Last follow-up date


Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2015 Year 07 Month 06 Day

Last modified on

2015 Year 07 Month 06 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000020665


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name