UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000030735
Receipt number R000034581
Scientific Title Diagnostic accuracy of contrast enhanced endoscopic ultrasonography in pancreatbiliary disease
Date of disclosure of the study information 2018/01/15
Last modified on 2019/07/12 10:09:40

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Basic information

Public title

Diagnostic accuracy of contrast enhanced endoscopic ultrasonography in pancreatbiliary disease

Acronym

A clinical trial of contrast enhanced endoscopic ultrasonography in the pancreatobiliary disease

Scientific Title

Diagnostic accuracy of contrast enhanced endoscopic ultrasonography in pancreatbiliary disease

Scientific Title:Acronym

A clinical trial of contrast enhanced endoscopic ultrasonography in the pancreatobiliary disease

Region

Japan


Condition

Condition

Pancreas tumor, Chronic pancreatitis, Autoimmune pancreatitis, Gallblader polyp, Biliary tract tumor

Classification by specialty

Hepato-biliary-pancreatic medicine

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

The aim of the present study is to evaluate whether contrast-enhanced endoscopic ultrasonography can provide a reliable diagnosis for pancreatobbiliary disease.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

To evaluate whether contrast enhanced endoscopic ultrasonography can provide a reliable diagnosis for pancreatobbiliary disease, we compare the diagnostic accuracy of contrast enhanced endoscopic ultrasonography with enhanced conputed tomography, magnetic resonance imaging, and endoscopic ultrasonography without perflubutane

Key secondary outcomes



Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Non-randomized

Randomization unit


Blinding

Double blind -all involved are blinded

Control

Active

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

4

Purpose of intervention

Diagnosis

Type of intervention

Medicine

Interventions/Control_1

Contrast enhanced endoscopic ultrasonography using perflubutane

Interventions/Control_2

MRI

Interventions/Control_3

enhanced CT

Interventions/Control_4

endoscopic ultrasonography without perflubutane

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

100 years-old >=

Gender

Male and Female

Key inclusion criteria

1.Patients who are suspected pacreatobiliary disease by ohter modality(CT, US, MRI).
2.Performance status; 0,1,2.
3.Patients who got ingormed consent.

Key exclusion criteria

1.Patients with allergy to egg.
2.Patients with arteriovenous shunt in cardia.
3.Patients woth severe cardiac disease.
4.Patients with sebere lung disorder.
5.Female patients with pregnacy or nursing.
6.Patients with mental aliments who cannot sign up for this clinical trial.
7.Patients with adverse events to perflubutane including minimal side effects.
8.Inadequate patients to participate in this study, in the judgement of an attending doctor or inspection physician.

Target sample size

786


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Kazuki Sumiyama

Organization

The Jikei University School of Medicine

Division name

Department of Endoscopy

Zip code


Address

3-25-8, Nishi-Shinbashi, Minato-ku, Tokyo, Japan

TEL

0334331111

Email

kaz_sum@jikei.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Masafumi Chiba

Organization

The Jikei University School of Medicine

Division name

Department of Endoscopy

Zip code


Address

3-25-8, Nishi-Shinbashi, Minato-ku, Tokyo, Japan

TEL

0334331111

Homepage URL


Email

ccl09720@gmail.com


Sponsor or person

Institute

Department of Endoscopy
The Jikei University School of Medicine

Institute

Department

Personal name



Funding Source

Organization

Department of Endoscopy
The Jikei University School of Medicine

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

東京慈恵会医科大学附属病院(東京都)、東京慈恵会医科大学附属柏病院(千葉県)、東京慈恵会医科大学葛飾医療センター(東京都)、東京慈恵会医科大学附属第三病院(東京都)


Other administrative information

Date of disclosure of the study information

2018 Year 01 Month 15 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

2017 Year 11 Month 14 Day

Date of IRB

2018 Year 11 Month 14 Day

Anticipated trial start date

2018 Year 01 Month 15 Day

Last follow-up date

2019 Year 03 Month 31 Day

Date of closure to data entry

2019 Year 03 Month 31 Day

Date trial data considered complete

2019 Year 03 Month 31 Day

Date analysis concluded

2019 Year 03 Month 31 Day


Other

Other related information



Management information

Registered date

2018 Year 01 Month 09 Day

Last modified on

2019 Year 07 Month 12 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000034581


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name