UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000011113
Receipt number R000013020
Scientific Title A study on the classification of inflammatory bowel disease by the patterns of immunological profiles
Date of disclosure of the study information 2013/07/04
Last modified on 2020/07/09 16:07:17

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Basic information

Public title

A study on the classification of inflammatory bowel disease by the patterns of immunological profiles

Acronym

Classification of inflammatory bowel disease by the patterns of immunological profiles

Scientific Title

A study on the classification of inflammatory bowel disease by the patterns of immunological profiles

Scientific Title:Acronym

Classification of inflammatory bowel disease by the patterns of immunological profiles

Region

Japan


Condition

Condition

Crohn's Disease, ulcerative colitis

Classification by specialty

Gastroenterology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

In this study, the array of immunological makers, such as cytokines and chemokines, will be measured in the intestinal tissue and the serum samples of patients with inflammatory bowel disease (ulcerative colitis and Crohn's disease) and healthy volunteers to test if those diseases can be categorized into subgroups by the patterns of immunological skewing.

Basic objectives2

Others

Basic objectives -Others

1. Classification of inflammatory bowel disease by the patterns of immunological profiles.
2. The feasibility of the immunological classification of inflammatory bowel disease for the selection of proper therapeutic strategy.

Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

The immunological profiling will be determined by the measurement of cytokines, chemokines and other factors in the serum and intestinal tissue samples. The patients will be classified into subgroups by the immunological features, and the correlation of endoscopical disease activity, clinical course, and the responsiveness and/or resistance to therapy protocol with those subgroups will be analyzed.

Key secondary outcomes

The feasibility of immunological profiling for the selection of proper therapeutic strategy and prediction of the clinical course.


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

Diagnosis

Type of intervention

Maneuver

Interventions/Control_1

5 ml of blood sample and 3 biopsy samples of the intestinal tissue will be collected from each person.

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

80 years-old >

Gender

Male and Female

Key inclusion criteria

Patients with inflammatory bowel disease and healthy volunteers.

Key exclusion criteria

[Patients]
Pregnant women are excluded.
Patients who have obvious intestinal disease and/or systemic inflammation caused by other than inflammatory bowel disease, such as advanced cancer, systemic autoimmune disease, and infections are excluded.
Patients with bleeding tendency are excluded.
[Healthy volunteers]
Pregnant women are excluded.
Persons with bleeding tendency are excluded.

Target sample size

120


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Namiko Hoshi

Organization

Kobe University Graduate School of Medicine

Division name

Gastroenterology

Zip code


Address

7-5-1 Kusunoki, Chuo-Ward, Kobe, Japan

TEL


Email



Public contact

Name of contact person

1st name
Middle name
Last name Namiko Hoshi

Organization

Kobe University Graduate School of Medicine

Division name

Gastroenterology

Zip code


Address


TEL

078-382-5774

Homepage URL


Email



Sponsor or person

Institute

Kobe University Graduate School of Medicine

Institute

Department

Personal name



Funding Source

Organization

MEXT(Japan)

Organization

Division

Category of Funding Organization

Nationality of Funding Organization

Japan


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

2013 Year 07 Month 04 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

2013 Year 06 Month 11 Day

Date of IRB

2013 Year 06 Month 11 Day

Anticipated trial start date

2013 Year 06 Month 12 Day

Last follow-up date

2019 Year 01 Month 11 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2013 Year 07 Month 04 Day

Last modified on

2020 Year 07 Month 09 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000013020


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name