UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000006857
Receipt number R000008109
Scientific Title A prospective study of endoscopic ultrasound-guided hepaticogastrostomy in patients with a surgically altered upper gastrointestinal tract
Date of disclosure of the study information 2011/12/08
Last modified on 2017/06/10 10:20:55

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Basic information

Public title

A prospective study of endoscopic ultrasound-guided hepaticogastrostomy in patients with a surgically altered upper gastrointestinal tract

Acronym

EUS-HGS for patients with a surgically altered GI tract

Scientific Title

A prospective study of endoscopic ultrasound-guided hepaticogastrostomy in patients with a surgically altered upper gastrointestinal tract

Scientific Title:Acronym

EUS-HGS for patients with a surgically altered GI tract

Region

Japan


Condition

Condition

Unresectable malignant biliary obstruction with a surgically altered uuper gastrointestinal tract

Classification by specialty

Hepato-biliary-pancreatic medicine

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

To evaluate the feasibility and safety of EUS-HGS

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

A technical and clinical success rate

Key secondary outcomes

Complications, Time to dysfunction


Base

Study type

Observational


Study design

Basic design


Randomization


Randomization unit


Blinding


Control


Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms


Purpose of intervention


Type of intervention


Interventions/Control_1


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)Unresectable malignant biliary obsturction
2)T-Bil > 3.0mg/dl
3)Performance status(PS) Grade 0-3
4)Age >20years
5)Written informed consent was obrained

Key exclusion criteria

1)Billroth I or II reconstruction
2)Severe cholangitis
3)Ileus
4)Severe cardio-respiratory failure
5)Severe renal failure
6)Steroid therapy(PSL5mg/dl more than 1 month)
7)Severe ascites
8)Severe bleeding diathesis
9)Imparied conciousness (>JCS I-1)
10)Severe cardiac diseases
11)Severe respiratory disease
12)Pregnant women

Target sample size

20


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Hiroyuki Isayama

Organization

Graduate School of Medicine, The University of Tokyo

Division name

Gastroenterology

Zip code


Address

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

TEL


Email



Public contact

Name of contact person

1st name
Middle name
Last name

Organization

Graduate School of Medicine, The University of Tokyo

Division name

Gastroenterology

Zip code


Address

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

TEL


Homepage URL


Email



Sponsor or person

Institute

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

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



Other administrative information

Date of disclosure of the study information

2011 Year 12 Month 08 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

Open public recruiting

Date of protocol fixation

2011 Year 11 Month 04 Day

Date of IRB


Anticipated trial start date

2011 Year 12 Month 01 Day

Last follow-up date


Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

None


Management information

Registered date

2011 Year 12 Month 07 Day

Last modified on

2017 Year 06 Month 10 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000008109


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name