UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000020057
Receipt number R000023159
Scientific Title Clinical Study of Thoracic Endovascular Repair for Aortic Arch Aneurysms with Surgeon-Modified Fenestrated and Retrograde Branched Device
Date of disclosure of the study information 2015/12/03
Last modified on 2021/12/07 10:40:25

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Basic information

Public title

Clinical Study of Thoracic Endovascular Repair for Aortic Arch Aneurysms with Surgeon-Modified Fenestrated and Retrograde Branched Device

Acronym

Clinical Study of Thoracic Endovascular Repair for Aortic Arch Aneurysms with Surgeon-Modified Fenestrated and Retrograde Branched Device

Scientific Title

Clinical Study of Thoracic Endovascular Repair for Aortic Arch Aneurysms with Surgeon-Modified Fenestrated and Retrograde Branched Device

Scientific Title:Acronym

Clinical Study of Thoracic Endovascular Repair for Aortic Arch Aneurysms with Surgeon-Modified Fenestrated and Retrograde Branched Device

Region

Japan


Condition

Condition

Aortic Arch or Distal Arch Aneurysms

Classification by specialty

Vascular surgery Radiology Cardiovascular surgery

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

The aim of the study is to evaluate the peri-operative clinical outcomes and
long-term clinical outcomes of thoracic endovascular repair for aortic arch aneurysms with surgeon-modified fenestrated and retrograde branched device

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1

Confirmatory

Trial characteristics_2

Pragmatic

Developmental phase

Not applicable


Assessment

Primary outcomes

The rates of aortic disease related
death at 12 months post-procedure

Key secondary outcomes

Device Success, Procedural Time, Condit Usage During The Procedure, Clinical Utility Measures, Morbidity, Including The Composite Rate Of Major Adverse Events, Endoleak, Change In Aneurysm Size, Migration, Device Patency, Device Integrity


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

Treatment

Type of intervention

Device,equipment

Interventions/Control_1

Treat aortic arch aneurysms with surgeon-modified fenestrated and retrograde branched stent graft and follow up with patients for 12 months post-operatively.

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

1) Aortic arch fusiform aneurysm with diameter >50 mm
2) Aortic arch fusiform aneurysm with a history of growth >5 mm per year
3) Aortic arch saccular aneurysm with 1.5 times the diameter as compared to the normal size

Key exclusion criteria

<General Exclusion Criteria>
1) Less than 20 years of age
2) Pregnant or patients likely to have been pregnant
3) Life expectancy less than 1 years
4) Unwilling to company with the follow up schedule
5) Inability or refusal to give informed consent

*Additionally, there is Medical Exclusion Criteria and Anatomical Exclusion Criteria, too.

Target sample size

25


Research contact person

Name of lead principal investigator

1st name Satoshi
Middle name
Last name Satoshi

Organization

Shimane Prefectural Central Hospital

Division name

Department of Cardiovascular Surgery

Zip code

6938555

Address

4-1-1 Himebara, Izumo City, Shimane, Japan

TEL

0853-22-5111

Email

kamihira@spch.izumo.shimane.jp


Public contact

Name of contact person

1st name Satoshi
Middle name
Last name Satoshi

Organization

Shimane Prefectural Central Hospital

Division name

Department of Cardiovascular Surgery

Zip code

6938555

Address

4-1-1 Himebara, Izumo City, Shimane, Japan

TEL

0853-22-5111

Homepage URL


Email

kamihira@spch.izumo.shimane.jp


Sponsor or person

Institute

Shimane Prefectural Central Hospital

Institute

Department

Personal name



Funding Source

Organization

Shimane Prefectural Central Hospital

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

Shimane Prefectural Central Hospital

Address

4-1-1 Himebara, Izumo City, Shimane, Japan

Tel

0853-22-5111

Email

chiken@spch.izumo.shimane.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

2015 Year 12 Month 03 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

15

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

2015 Year 07 Month 06 Day

Date of IRB

2015 Year 07 Month 31 Day

Anticipated trial start date

2015 Year 08 Month 01 Day

Last follow-up date

2021 Year 08 Month 01 Day

Date of closure to data entry

2021 Year 08 Month 01 Day

Date trial data considered complete

2021 Year 08 Month 01 Day

Date analysis concluded

2021 Year 08 Month 01 Day


Other

Other related information



Management information

Registered date

2015 Year 12 Month 03 Day

Last modified on

2021 Year 12 Month 07 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000023159


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name