UMIN-ICDS Clinical Trial

Unique ID issued by UMIN UMIN000051426
Receipt number R000058665
Scientific Title Verification and identification of new biomarkers for intestinal barrier function
Date of disclosure of the study information 2023/06/23
Last modified on 2024/03/22 15:53:50

* This page includes information on clinical trials registered in UMIN clinical trial registed system.
* We don't aim to advertise certain products or treatments


Basic information

Public title

Verification and identification of new biomarkers for intestinal barrier function

Acronym

Verification and identification of new biomarkers for intestinal barrier function

Scientific Title

Verification and identification of new biomarkers for intestinal barrier function

Scientific Title:Acronym

Verification and identification of new biomarkers for intestinal barrier function

Region

Japan


Condition

Condition

Healthy Adults

Classification by specialty

Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

Verification of the efficacy of biomarkers discovered in previous studies and identification for new biomarkers

Basic objectives2

Others

Basic objectives -Others

Verification of the efficacy of biomarkers discovered in previous studies and identification for new biomarkers.

Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Verification of the efficacy of biomarkers discovered in previous studies. Identification for new biomarkers from this study.

Key secondary outcomes

Investigation of changes in biomarkers with yogurt intake.


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

75 years-old >

Gender

Male and Female

Key inclusion criteria

1. Subjects underwent a pre-ingestion test among the study subjects in the study in which the specimen was obtained
2. Subjects who did not request withdrawal from participation in this study

Key exclusion criteria

1. Subjects whose samples (plasma, urine, stool) have not been obtained at all

Target sample size

150


Research contact person

Name of lead principal investigator

1st name Masashi
Middle name
Last name Morifuji

Organization

Meiji Co., Ltd.

Division name

R&D Division

Zip code

192-0919

Address

1-29-1 Nanakuni, Hachiouji, Tokyo, Japan

TEL

81-42-632-5838

Email

masashi.morifuji@meiji.com


Public contact

Name of contact person

1st name Eiji
Middle name
Last name Yoshikawa

Organization

KSO Corporation

Division name

Sales department

Zip code

105-0023

Address

1-9-7, Shibaura, Minato-ku, Tokyo The 7th floor of Shibaura omodaka building

TEL

81-3-3452-7733

Homepage URL


Email

eigyou27@kso.co.jp


Sponsor or person

Institute

Meiji Co., Ltd.

Institute

Department

Personal name



Funding Source

Organization

Meiji Co., Ltd.

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

Ethical Committee of Kobuna Orthopedics Clinic

Address

311-2 Gokan-machi, Maebashi-shi, Gunma, Japan

Tel

027-261-7600

Email

info@kobunaseikei.jp


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

2023 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

149

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

2022 Year 12 Month 14 Day

Date of IRB

2022 Year 12 Month 26 Day

Anticipated trial start date

2023 Year 06 Month 23 Day

Last follow-up date

2024 Year 03 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

untargeted metabolomics


Management information

Registered date

2023 Year 06 Month 23 Day

Last modified on

2024 Year 03 Month 22 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/icdr_e/ctr_view.cgi?recptno=R000058665


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name