UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000006748
Receipt number R000007977
Scientific Title Efficacy of Hydrocoil on endovascular treatment for intracranial aneurysms; Multi-center, prospective, randomized, open-label blind-endpoint trial
Date of disclosure of the study information 2011/12/21
Last modified on 2019/10/08 17:12:37

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Basic information

Public title

Efficacy of Hydrocoil on endovascular treatment for intracranial aneurysms; Multi-center, prospective, randomized, open-label blind-endpoint trial

Acronym

HYBRID (HYdrocoil versus Bare platinum coil in Recanalization Imaging Data) study

Scientific Title

Efficacy of Hydrocoil on endovascular treatment for intracranial aneurysms; Multi-center, prospective, randomized, open-label blind-endpoint trial

Scientific Title:Acronym

HYBRID (HYdrocoil versus Bare platinum coil in Recanalization Imaging Data) study

Region

Japan


Condition

Condition

Intracranial anerysm

Classification by specialty

Radiology Neurosurgery

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To compare Hydrocoil and bare platinum coil for recanalization after endovascular treatment of intracranial aneurysms.

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1

Confirmatory

Trial characteristics_2

Pragmatic

Developmental phase

Not applicable


Assessment

Primary outcomes

recanalization within 1 year after embolization

Key secondary outcomes

1. aneurysmal rupture within 1 year after embolization
2. any event within 30 days after embolization
3. recanalization within 6 months after embolization
4. aneurysmal retreatment within 1 year after embolization
5. aneurysmal rupture and any death within 1 year after embolization
6. any stroke within 1 year after embolization
7. any stroke, death hemorrhagic event, aneurysmal recanalization or retreatment within 1 year after embolization
8. change in aneurysmal occlusion
9. any comlicaion within 1 year after embolization
10. %length of Hydrocoil, maximum diameter of aneurysm, volume embolization ratio


Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit

Individual

Blinding

Open -but assessor(s) are blinded

Control

Active

Stratification

YES

Dynamic allocation

NO

Institution consideration

Institution is considered as adjustment factor in dynamic allocation.

Blocking

NO

Concealment

Central registration


Intervention

No. of arms

2

Purpose of intervention

Treatment

Type of intervention

Device,equipment

Interventions/Control_1

Hydrocoil

Interventions/Control_2

Bare Platinum Coil

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

80 years-old >

Gender

Male and Female

Key inclusion criteria

1. saccular intracranial aneurysm
2. endovascular treatment scheduled within 60days after consent
3. 20-79 years old
4. unruptured, chronic SAH or acurte SAH Grade 1-III
5. 7-20mm in size
6. 1 year follow up possibel
7. independent (mRS 0-2)
8. document consent

Key exclusion criteria

1. previous endovascular treated
2. additional aneurysm scheduled of endovascular treatment
3. pregnant
4. ineligible for study

Target sample size

500


Research contact person

Name of lead principal investigator

1st name Nobuyuki
Middle name
Last name Sakai

Organization

Kobe City Medical Center General Hospital

Division name

Neurosurgery

Zip code

650-0047

Address

2-1-1 Minatojima-Minamimachi, Chuo-ku, Kobe, 650-0047 Japan

TEL

078-302-4321

Email

n.sakai@siren.ocn.ne.jp


Public contact

Name of contact person

1st name Nobuyuki
Middle name
Last name Sakai

Organization

Kobe City Medical Center general Hospital

Division name

Neurosurgery

Zip code

650-0047

Address

2-1-1 Minatojima-Minamimachi, Chuo-ku, Kobe, 650-0047 Japan

TEL

078-302-4321

Homepage URL


Email

n.sakai@siren.ocn.ne.jp


Sponsor or person

Institute

Transitional Research Informatics Center

Institute

Department

Personal name



Funding Source

Organization

Transitional Research Informatics Center

Organization

Division

Category of Funding Organization

Non profit foundation

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Kobe City Medical Center General Hospital

Address

2-1-1 Minatojima-Minamimachi, Chuo-ku, Kobe, 650-0047 Japan

Tel

078-302-4321

Email

rinken@kcho.jp


Secondary IDs

Secondary IDs

YES

Study ID_1

NCT01516658

Org. issuing International ID_1

ClinicalTrials.gov

Study ID_2


Org. issuing International ID_2


IND to MHLW



Institutions

Institutions

神戸市立医療センター中央市民病院(兵庫県)、中村記念病院(北海道)、仙台医療センター(宮城県)、広南病院(宮城県)、獨協医科大学越谷病院(埼玉県)、千葉県救命救急センター(千葉県)、千葉大学(千葉県)、虎の門病院(東京都)、東京医科歯科大学(東京都)、新潟大学(新潟県)、富山大学(富山県)、信州大学(長野県)、名古屋大学(愛知県)、岐阜大学(岐阜県)、京都大学(京都府)、大阪大学(大阪府)、国立循環器病研究センター(大阪府)、和歌山労災病院(和歌山県)、岡山大学(岡山県)、山口大学(山口県)、香川大学(香川県)、徳島大学(徳島県)、小倉記念病院(福岡県)、福岡大学(福岡県)、久留米大学(福岡県)


Other administrative information

Date of disclosure of the study information

2011 Year 12 Month 21 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

437

Results


Results date posted


Results Delayed

Delay expected

Results Delay Reason

not yet reported

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

2011 Year 11 Month 11 Day

Date of IRB

2011 Year 11 Month 20 Day

Anticipated trial start date

2012 Year 01 Month 01 Day

Last follow-up date

2018 Year 03 Month 31 Day

Date of closure to data entry

2018 Year 09 Month 30 Day

Date trial data considered complete

2019 Year 03 Month 31 Day

Date analysis concluded

2019 Year 09 Month 30 Day


Other

Other related information



Management information

Registered date

2011 Year 11 Month 20 Day

Last modified on

2019 Year 10 Month 08 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000007977


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name