UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000011618
Receipt number R000013508
Scientific Title Safety and efficacy of endosaccular embolization of visceral aneurysms using Hydrocoils: a multicenter study
Date of disclosure of the study information 2013/09/01
Last modified on 2021/03/08 12:49:34

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Basic information

Public title

Safety and efficacy of endosaccular embolization of visceral aneurysms using Hydrocoils: a multicenter study

Acronym

Endosaccular embolization of visceral aneurysms using Hydrocoils: a multicenter study

Scientific Title

Safety and efficacy of endosaccular embolization of visceral aneurysms using Hydrocoils: a multicenter study

Scientific Title:Acronym

Endosaccular embolization of visceral aneurysms using Hydrocoils: a multicenter study

Region

Japan


Condition

Condition

Vesceral aneurysms

Classification by specialty

Radiology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To determine the safety and efficacy (effects on volume embolization ratio and prevention of recanalization) of endosaccular embolization using Hydrocoils in comparison with embolization using bare platinum coils

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Volume embolozation ratio
Embolization effect 1 year after treatment

Key secondary outcomes



Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit

Individual

Blinding

Single blind -participants are blinded

Control

Active

Stratification


Dynamic allocation

YES

Institution consideration


Blocking


Concealment



Intervention

No. of arms

2

Purpose of intervention

Treatment

Type of intervention

Device,equipment

Interventions/Control_1

Hydrogel-coating coil group

Interventions/Control_2

Non-hydrogel coating coil group (Bare platinum coil group)

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. Unruptured visceral artery aneurysm which can be treated by endosaccular coil embolization
2. Patients aged 20 or over at the time of informed consent

Key exclusion criteria

1. Diameter of aneurysm is less than 10mm
2. Diameter of aneurysm is larger than 30mm
3. A case treated by using metallic stent
4. A case with active bleeding
5. A case with active infective disease
6. A case with active asthma and/or severe allergic disease
7. A case with congestive heart failure
8. A case with blood disease
9. A case with severe hepatic and/or renal disease
10. A case with uncontrollable malignant disease
11. Pregnant
12. A case whose performance status is over 3
13. WBC count is less than 2000 or granulocyte count is less than 1000
14. Platelet count is less than 50,000/mm3 or PT-INR is over 1.5
15. A case deemed to be inadequate for this study

Target sample size

80


Research contact person

Name of lead principal investigator

1st name Hiro
Middle name
Last name Kiyosue

Organization

Oita University Faculty of Medicine

Division name

Radiology

Zip code

879-5593

Address

Idaigaoka, 1-1, Hasama-machi, Yufu-shi, Oita

TEL

097-586-5934

Email

hkiyosue@oita-u.ac.jp


Public contact

Name of contact person

1st name Tanoue
Middle name
Last name Shuichi

Organization

Oita University Faculty of Medicine

Division name

Radiology

Zip code

879-5593

Address

Idaigaoka, 1-1, Hasama-machi, Yufu-shi, Oita

TEL

097-586-5934

Homepage URL


Email

stanoue@oita-u.ac.jp


Sponsor or person

Institute

Department of Radiology, Oita University Faculty of Medicine

Institute

Department

Personal name



Funding Source

Organization

Department of Radiology, Oita University Faculty 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

Department of Radiology, Oita University Faculty of Medicine

Address

Idaigaoka, 1-1, Yufu-shi, Oita, 879-5593, Japan

Tel

097-586-5934

Email

radioogy@oita-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

大分大学,慶応大学,大阪大学,奈良県立医科大学,久留米大学


Other administrative information

Date of disclosure of the study information

2013 Year 09 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

No longer recruiting

Date of protocol fixation

2013 Year 08 Month 01 Day

Date of IRB

2016 Year 07 Month 27 Day

Anticipated trial start date

2013 Year 08 Month 31 Day

Last follow-up date

2020 Year 07 Month 27 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 09 Month 01 Day

Last modified on

2021 Year 03 Month 08 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000013508


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name