UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000020435
Receipt number R000023604
Scientific Title Endovascular treatment using N-Butyl Cyanoacrylate (NBCA) liquid adhesive for arteriovenous malformations, dural arteriovenous fistulas and brain tumors
Date of disclosure of the study information 2016/01/05
Last modified on 2016/01/17 12:28:57

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Basic information

Public title

Endovascular treatment using N-Butyl Cyanoacrylate (NBCA) liquid adhesive for arteriovenous malformations, dural arteriovenous fistulas and brain tumors

Acronym

Endovascular treatment using NBCA for arteriovenous malformations, dural arteriovenous fistulas and brain tumors

Scientific Title

Endovascular treatment using N-Butyl Cyanoacrylate (NBCA) liquid adhesive for arteriovenous malformations, dural arteriovenous fistulas and brain tumors

Scientific Title:Acronym

Endovascular treatment using NBCA for arteriovenous malformations, dural arteriovenous fistulas and brain tumors

Region

Japan


Condition

Condition

arteriovenous malformations, dural arteriovenous fistulas and brain tumors

Classification by specialty

Neurosurgery

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To determine the influence of endovascular treatment using N-Butyl Cyanoacrylate (NBCA) liquid adhesive for arteriovenous malformations, dural arteriovenous fistulas and brain tumors

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1

Confirmatory

Trial characteristics_2

Pragmatic

Developmental phase

Not applicable


Assessment

Primary outcomes

Evaluation for the endovascular treatment using NBCA for the feeding arteries
The treatment next day: MRI

Key secondary outcomes

Occurrence of the treatment complication and adverse event


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

Medicine

Interventions/Control_1

treatment using NBCA
The dosage period: during the endovascular treatment
The dosage:0.1ml-0.5ml NBCA per feeding artery
The dosage number of times: 1-5 feeding arteries

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


Not applicable

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

1. large size arteriovenous malformations could not operated simply or radiosurgery simply
2. dural arteriovenous malformations could not reached by transvenous approach
3. large brain tumors that have vascular feeders

Key exclusion criteria

the cases whose feeding arteries could not reached by micro catheters

Target sample size

20


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Naked Mitsutoshi

Organization

Graduate School of Medical Science Kanazawa university

Division name

Department of Neurosurgery

Zip code


Address

13-1 Takara-machi, Kanazawa, Ishikawa

TEL

076-265-2384

Email

mnakada@med.kanazawa-u.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Mohri Masanao

Organization

Graduate School of Medical Science Kanazawa university

Division name

Department of Neurosurgery

Zip code


Address

13-1 Takara-machi, Kanazawa, Ishikawa

TEL

076-265-2384

Homepage URL


Email

mmohri@med.kanazawa-u.ac.jp


Sponsor or person

Institute

Uchiyama Naoyuki
Mohri Masanao
Misaki Kouichi

Institute

Department

Personal name



Funding Source

Organization

none

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


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

金沢大学病院(石川県)


Other administrative information

Date of disclosure of the study information

2016 Year 01 Month 05 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

Enrolling by invitation

Date of protocol fixation

2014 Year 02 Month 24 Day

Date of IRB


Anticipated trial start date

2015 Year 06 Month 17 Day

Last follow-up date

2016 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

2016 Year 01 Month 05 Day

Last modified on

2016 Year 01 Month 17 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000023604


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name