UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000010374
Receipt number R000012139
Scientific Title Transfusion criteria for fresh frozen plasma in liver resection.
Date of disclosure of the study information 2013/04/08
Last modified on 2020/04/06 13:33:13

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Basic information

Public title

Transfusion criteria for fresh frozen plasma in liver resection.

Acronym

Criteria for FFP in liver resection.

Scientific Title

Transfusion criteria for fresh frozen plasma in liver resection.

Scientific Title:Acronym

Criteria for FFP in liver resection.

Region

Japan


Condition

Condition

The patients who recieve liver resection.

Classification by specialty

Hepato-biliary-pancreatic surgery

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

To establish transfusion criteria for use of fresh frozen plasma in liver resection.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

increase of middle grade postoperative complication without FFP.

Key secondary outcomes



Base

Study type


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

Treatment

Type of intervention

Medicine

Interventions/Control_1

A dose-escalation design which commonly used in phase I study is applied with some modifications. The starting step of PT-INR value is 1.5 (Step 1), which is added every 0.1 by step: ex. 1.6 (Step 2), 1.7 (Step 3).The step was proceeded until the post operative complication (POC) without transfusion was occurred or PT-INR is 3.0.

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

100 years-old >=

Gender

Male and Female

Key inclusion criteria

The patinets who undergo liver resection.

Key exclusion criteria

Otherserious medical illnesses which conditions cannot be rescued without FFP.

Target sample size

150


Research contact person

Name of lead principal investigator

1st name Takafumi
Middle name
Last name Kumamoto

Organization

Yokohama City University Graduate School of Medicine

Division name

Department of Gastroenterological Surgery

Zip code

236-0004

Address

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

TEL

045-787-2650

Email

t.kumamoto@k5.dion.ne.jp


Public contact

Name of contact person

1st name Takafumi
Middle name
Last name Kumamoto

Organization

Yokohama City University Graduate School of Medicine

Division name

Department of Gastroenterological Surgery

Zip code

2360004

Address

3-9 Fukuura, Kanazawa-Ku, Yokohama 236-0004 Japan

TEL

045-787-2650

Homepage URL


Email

t.kumamoto@k5.dion.ne.jp


Sponsor or person

Institute

Yokohama City University Graduate School of Medicine

Institute

Department

Personal name



Funding Source

Organization

Department of Gastroenterological Surgery,
Yokohama City University Graduate School of Medicine

Organization

Division

Category of Funding Organization

Self funding

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Yokohama City University Graduate School of Medicine

Address

3-9 Fukuura, Kanazawa-Ku, Yokohama 236-0004 Japan

Tel

0457872650

Email

t.kumamoto@k5.dion.ne.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

2013 Year 04 Month 08 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

Terminated

Date of protocol fixation

2013 Year 03 Month 31 Day

Date of IRB

2013 Year 03 Month 31 Day

Anticipated trial start date

2013 Year 04 Month 08 Day

Last follow-up date

2018 Year 03 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2013 Year 03 Month 31 Day

Last modified on

2020 Year 04 Month 06 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000012139


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name