UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000011608
Receipt number R000013580
Scientific Title Feasibility and efficacy of novel EUS-guided gastrojejunostomy technique using a new double-balloon enteric tube and lumen-apposing metal stent
Date of disclosure of the study information 2013/08/30
Last modified on 2015/05/22 20:01:19

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Basic information

Public title

Feasibility and efficacy of novel EUS-guided gastrojejunostomy technique using a new double-balloon enteric tube and lumen-apposing metal stent

Acronym

Feasibility and efficacy of novel EUS-GJ technique

Scientific Title

Feasibility and efficacy of novel EUS-guided gastrojejunostomy technique using a new double-balloon enteric tube and lumen-apposing metal stent

Scientific Title:Acronym

Feasibility and efficacy of novel EUS-GJ technique

Region

Japan Asia(except Japan)


Condition

Condition

Malignant gastric outlet obstruction

Classification by specialty

Gastroenterology Hepato-biliary-pancreatic medicine

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

To evaluate a novel double-balloon ileus tube and lumen-apposing stent designed for EUS-guided gastrojejunostomy.

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase

Phase I


Assessment

Primary outcomes

success rate

Key secondary outcomes

Frequency and kinds of complications and stent patency


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

Maneuver

Interventions/Control_1

EUS-guided gastrojejunostomy

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 in whom gastric outlet obstruction is present and surgical gastric jejunostomy or endoscoic duodenal stenting is required.
2) Patients consent to be included in the study based on his/her own free will after sufficient informing and understanding of the study.

Key exclusion criteria

1) Cases having difficulty in endoscopic approach
2) Cases having difficulty in EUS guided puncture
3) Cases with much ascites
4) Cases in Perfomance status 4
5) Cases with sever complication in other organs
6) Cases without informed consent
7) Cases judged by principal investigator to be inadequate as subjects

Target sample size

10


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Takao Itoi

Organization

Tokyo Medical University Hospital

Division name

Department of the 4th Internal medicine (Gastroenterology and Hepatology)

Zip code


Address

6-7-1 Nishishijuku, Shinjuku-ku, Tokyo 160-0023

TEL

03-3342-6111

Email

itoi@tokyo-med.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Takao Itoi

Organization

Tokyo Medical University Hospital

Division name

Department of the 4th Internal medicine (Gastroenterology and Hepatology)

Zip code


Address

6-7-1 Nishishijuku, Shinjuku-ku, Tokyo 160-0023

TEL

03-3342-6111

Homepage URL


Email

itoi@tokyo-med.ac.jp


Sponsor or person

Institute

Tokyo Medical University Hospital

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

Gastroenterology, Global Hospital (Mumbai, India)

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

東京医科大学病院(東京都)


Other administrative information

Date of disclosure of the study information

2013 Year 08 Month 30 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

Completed

Date of protocol fixation

2013 Year 08 Month 30 Day

Date of IRB


Anticipated trial start date

2013 Year 08 Month 30 Day

Last follow-up date


Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2013 Year 08 Month 30 Day

Last modified on

2015 Year 05 Month 22 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000013580


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name