UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000013291
Receipt number R000015464
Scientific Title Efficacy and safety of inside stent in patients with biliary stricture: a prospective multicenter study
Date of disclosure of the study information 2014/03/10
Last modified on 2019/09/02 12:46:26

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Basic information

Public title

Efficacy and safety of inside stent in patients with biliary stricture: a prospective multicenter study

Acronym

Multicenter Evolving Inside Stent Registry (MEISteR)

Scientific Title

Efficacy and safety of inside stent in patients with biliary stricture: a prospective multicenter study

Scientific Title:Acronym

Multicenter Evolving Inside Stent Registry (MEISteR)

Region

Japan


Condition

Condition

benign and malignant biliary stricture

Classification by specialty

Gastroenterology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To evaluate the efficacy and safety of inside stent for benign and malignant biliary stricture.

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1

Exploratory

Trial characteristics_2

Pragmatic

Developmental phase

Not applicable


Assessment

Primary outcomes

1) Stent patency period
2) Time to stent dysfunction

Key secondary outcomes

1) Technical success rate
2) Complication rate
3) resolution rate of benign biliary strictures


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

Inside stent

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) Patients with benign or malignant biliary stricture.
2) Patients with written informed consent.

Key exclusion criteria

1) Patients with less than 2cm distance between the papilla of Vater and biliary stricture.
2) Patients with tumor invasion to the papilla of Vater.
3) Patients with acute pancreatitis.
4) Patients with pregnancy or possible pregnancy.
5) Patients considered ineligible by the attending physician.

Target sample size

200


Research contact person

Name of lead principal investigator

1st name Hiroyuki
Middle name
Last name Isayama

Organization

Graduate School of Medicine, The University of Tokyo

Division name

Department of Gastroenterology

Zip code

113-8655

Address

7-3-1 Hongo, Bunkyo-ku, Tokyo

TEL

03-3815-5411

Email

isayama-tky@umin.ac.jp


Public contact

Name of contact person

1st name Hirofumi
Middle name
Last name Kogure

Organization

Secretariat of Inside Stent Study Group

Division name

Department of Gastroenterology, Graduate School of Medicine, The University of Tokyo

Zip code

113-8655

Address

7-3-1 Hongo, Bunkyo-ku, Tokyo

TEL

03-3815-5411

Homepage URL


Email

kogureh-tky@umin.ac.jp


Sponsor or person

Institute

Inside Stent Study Group

Institute

Department

Personal name



Funding Source

Organization

Gadelius Medical K.K.

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

Office for Human Research Studies (OHRS)

Address

7-3-1 Hongo, Bunkyo-ku, Tokyo

Tel

03-5841-0818

Email

ethics@m.u-tokyo.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

1. 東京大学医学部附属病院(東京都)
2. 北海道大学病院(北海道)
3. 札幌医科大学附属病院(北海道)
4. 手稲渓仁会病院(北海道)
5. 横浜市立大学附属市民総合医療センター(神奈川県)
6. 大阪赤十字病院(大阪府)
7. 岡山大学病院(岡山県)
8. JA尾道総合病院(広島県)
9. 久留米大学病院(福岡県)


Other administrative information

Date of disclosure of the study information

2014 Year 03 Month 10 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

134

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 02 Month 25 Day

Date of IRB

2014 Year 02 Month 24 Day

Anticipated trial start date

2014 Year 03 Month 10 Day

Last follow-up date

2016 Year 10 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

2014 Year 02 Month 26 Day

Last modified on

2019 Year 09 Month 02 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000015464


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name