UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000027906
Receipt number R000031970
Scientific Title Measurement of a novel serological marker for pancreatic cancer in esophageal, gastric, hepatic, bile duct and colorectal cancers
Date of disclosure of the study information 2017/06/23
Last modified on 2017/12/25 12:57:06

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Basic information

Public title

Measurement of a novel serological marker for pancreatic cancer in esophageal, gastric, hepatic, bile duct and colorectal cancers

Acronym

A specific diagnostic marker for pancreatic cancer

Scientific Title

Measurement of a novel serological marker for pancreatic cancer in esophageal, gastric, hepatic, bile duct and colorectal cancers

Scientific Title:Acronym

A specific diagnostic marker for pancreatic cancer

Region

Japan


Condition

Condition

Esohageal cancer, gastric cancer, hapatic cancer, bile duct cancer, colorectal cancer

Classification by specialty

Gastroenterology Hepato-biliary-pancreatic medicine

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

The aim of the present study is to assess whether 2 glycoproteins and 6 RNAs are specific diagnostic markers for pancreatic cancer.

Basic objectives2

Others

Basic objectives -Others

Confirmation of the diagnostic specificity against pancreatic cancer

Trial characteristics_1

Confirmatory

Trial characteristics_2


Developmental phase

Not applicable


Assessment

Primary outcomes

Comparison of the IGFP levels between patients of Esohageal, gastric, hapatic, bile duct, colorectal cancers and control individuals

Key secondary outcomes

Comparison of the area under the curve (AUC) of Reciever Operating Characteristic Curves (ROC curves) between IGFP and CA19-9


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

90 years-old >

Gender

Male and Female

Key inclusion criteria

(1) more than 20 years old and less than 90 years old
(2) patients of esophageal, gastric, hepatic, bile duct and colorectal cancers newly diagnosed and previously untreated
(3) all individuals classified as controls are diagnosed as chronic hepatitis or gastrointestinal diseases with being evaluated for non-pancreatic diseases.

Key exclusion criteria

(1) patients who were suffering from any kind of malignancies
(2) sever renal or liver dysfunction
(3) individuals who did not accept informed consent
(4) unsuitable individuals for this clinical study

Target sample size

100


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Keisuke Taniuchi

Organization

Kochi Medical School Hospital, Kochi University

Division name

Department of Gastroenterology and Hepatology

Zip code


Address

Kohasu, Oko-cho, Nankoku, Kochi

TEL

088-880-2339

Email

ktaniuchi@kochi-u.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Keisuke Taniuchi

Organization

Kochi Medical School Hospital, Kochi University

Division name

Department of Gastroenterology and Hepatology

Zip code


Address

Kohasu, Oko-cho, Nankoku, Kochi

TEL

088-880-2339

Homepage URL


Email

ktaniuchi@kochi-u.ac.jp


Sponsor or person

Institute

Department of Gastroenterology and Hepatology, Kochi Medical School, Kochi University

Institute

Department

Personal name



Funding Source

Organization

Ministry of Education, Culture, Sports, Science and Technology

Organization

Division

Category of Funding Organization

Japanese Governmental office

Nationality of Funding Organization



Other related organizations

Co-sponsor

Hata prefectural Hospital

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

2017 Year 06 Month 23 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

2017 Year 05 Month 19 Day

Date of IRB


Anticipated trial start date

2017 Year 05 Month 20 Day

Last follow-up date

2019 Year 03 Month 31 Day

Date of closure to data entry

2019 Year 04 Month 30 Day

Date trial data considered complete

2019 Year 05 Month 31 Day

Date analysis concluded

2019 Year 07 Month 31 Day


Other

Other related information

The identification code is given to individuals, and the data is resisted into EDC system (REDcap).


Management information

Registered date

2017 Year 06 Month 23 Day

Last modified on

2017 Year 12 Month 25 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000031970


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name