UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000008833
Receipt number R000010375
Scientific Title Endoscopic ultrasound-guided hepaticogastrostomy with a covered metal stent for malignant biliary obstruction: a prospective feasibility study
Date of disclosure of the study information 2012/09/01
Last modified on 2018/01/26 15:30:33

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Basic information

Public title

Endoscopic ultrasound-guided hepaticogastrostomy with a covered metal stent for malignant biliary obstruction: a prospective feasibility study

Acronym

EUS-HGS for malignant biliary obstruction

Scientific Title

Endoscopic ultrasound-guided hepaticogastrostomy with a covered metal stent for malignant biliary obstruction: a prospective feasibility study

Scientific Title:Acronym

EUS-HGS for malignant biliary obstruction

Region

Japan


Condition

Condition

Malignant biliary obstruction

Classification by specialty

Hepato-biliary-pancreatic medicine

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

To evaluate a safety and utility of EUS-HGS

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

A rate of stent dysfunction

Key secondary outcomes

Complication


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-HGS

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,Age>20
2,Patient without previous biliary drainage
3,Expected prognosis > 2 months
4,Performance status <2
5,Patients with written informed consent

Key exclusion criteria

1,Patients wihout intrahepatic bile duct dilation
2,Massive ascites
3,Severe comorbidity
4,Contraindications for upper GI endoscope
5,Severe biliary obstruction extending into secondary branch of left intrahepatic duct.
6,Bleeding diathesis

Target sample size

20


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Hiroshi Kawakami

Organization

Hokkaido University Hospital

Division name

Department of Gastroenterology

Zip code


Address

Kita14 Nishi5, Kita-ku, Sapporo

TEL


Email



Public contact

Name of contact person

1st name
Middle name
Last name

Organization

Hokkaido University Hospital

Division name

Clinical Research Support Center

Zip code


Address


TEL


Homepage URL


Email

crjimu@huhp.hokudai.ac.jp


Sponsor or person

Institute

Department of Gastroenterology, Hokkaido University Graduate School of Medicine

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

2012 Year 09 Month 01 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

Terminated

Date of protocol fixation

2012 Year 08 Month 15 Day

Date of IRB


Anticipated trial start date

2012 Year 09 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



Management information

Registered date

2012 Year 09 Month 01 Day

Last modified on

2018 Year 01 Month 26 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000010375


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name