UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000015986
Receipt number R000018593
Scientific Title RCT(randomized control trial) for effectiveness of Tranexamic acid for type II endoleak after endovascular aneurysm repair
Date of disclosure of the study information 2015/01/01
Last modified on 2018/12/20 09:19:40

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Basic information

Public title

RCT(randomized control trial) for effectiveness of Tranexamic acid for type II endoleak after endovascular aneurysm repair

Acronym

Tranexamic acid for type II endoleak

Scientific Title

RCT(randomized control trial) for effectiveness of Tranexamic acid for type II endoleak after endovascular aneurysm repair

Scientific Title:Acronym

Tranexamic acid for type II endoleak

Region

Japan


Condition

Condition

Abdominal aortic aneurysm

Classification by specialty

Vascular surgery

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To prove the reducing effect for type II endoleak in Tranexamic acid after EVAR

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Frequency of type II endoleak after EVAR (Number of patients)

Key secondary outcomes

1 Changing aneurysm size
2 Frequency of re-intervention
3 Biomarker

MMP-9
IFN-r
IL-6
D-dimer
FDP
PAI-1
TGF-B
PIC


Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit

Individual

Blinding

Open -no one is blinded

Control

No treatment

Stratification

YES

Dynamic allocation


Institution consideration


Blocking


Concealment

Central registration


Intervention

No. of arms

2

Purpose of intervention

Treatment

Type of intervention

Medicine

Interventions/Control_1

Tranexamic acid 750 mg/day for 6 months after EVAR

Interventions/Control_2

Non-administration of Tranexamic acid

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


Not applicable

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

EVAR cases for Abdominal aortic aneurysm Consent cases for this study

Key exclusion criteria

Rupture cases
History of thrombosis
Allergy for Tranexamic acid
Impossible for follow up

Target sample size

200


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Masaaki Kato

Organization

Morinomiya Hospital

Division name

Dept. of Cardiovascular Surgery

Zip code


Address

2-1-88 Morinomiya Joutou-ku Osaka 536-0025 Japan

TEL

06-6969-0111

Email

mkato3@gmail.com


Public contact

Name of contact person

1st name
Middle name
Last name Masaaki Kato

Organization

Morinomiya Hospital

Division name

Dept. of Cardiovascular Surgery

Zip code


Address

2-1-88 Morinomiya Joutou-ku Osaka 536-0025 Japan

TEL

06-6969-0111

Homepage URL


Email

mkato3@gmail.com


Sponsor or person

Institute

Morinomiya Hospital

Institute

Department

Personal name



Funding Source

Organization

Medtronic Japan Co., Ltd.

Organization

Division

Category of Funding Organization

Profit organization

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

森之宮病院(大阪府) Morinomiya Hospital(Osaka)


Other administrative information

Date of disclosure of the study information

2015 Year 01 Month 01 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

Completed

Date of protocol fixation

2014 Year 10 Month 01 Day

Date of IRB


Anticipated trial start date

2015 Year 06 Month 22 Day

Last follow-up date

2018 Year 03 Month 31 Day

Date of closure to data entry

2018 Year 03 Month 31 Day

Date trial data considered complete

2018 Year 03 Month 31 Day

Date analysis concluded

2018 Year 03 Month 31 Day


Other

Other related information



Management information

Registered date

2014 Year 12 Month 18 Day

Last modified on

2018 Year 12 Month 20 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000018593


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name