UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000056103
Receipt number R000064104
Scientific Title Exploratory study on the urinary biomarkers of food intake
Date of disclosure of the study information 2024/11/08
Last modified on 2024/11/08 15:45:20

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Basic information

Public title

Exploratory study on the urinary biomarkers of food intake

Acronym

Exploratory study on the urinary biomarkers of food intake

Scientific Title

Exploratory study on the urinary biomarkers of food intake

Scientific Title:Acronym

Exploratory study on the urinary biomarkers of food intake

Region

Japan


Condition

Condition

Healthy Adults

Classification by specialty

Not applicable

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

A comprehensive analysis and evaluation of urinary biomarkers before and after intake for a vinegar intake group taking vinegar for 4 weeks, a natto intake group taking natto for 1 week, and a yellow pea intake group taking yellow peas for 1 week

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Urinary Biomarkers after the non-intake period and after the intake period of the test food

Key secondary outcomes

Dietary assessment during the non-intake period and during the intake period of the test food


Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Non-randomized

Randomization unit


Blinding

Single blind -investigator(s) and assessor(s) are blinded

Control

Active

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

3

Purpose of intervention

Prevention

Type of intervention

Food

Interventions/Control_1

After 2 days of not taking vinegar, intake 100ml (twice a day) of vinegar for 4 weeks

Interventions/Control_2

After 2 weeks of not taking natto, intake 45g (once a day) of natto for 1 weeks

Interventions/Control_3

After 2 weeks of not taking yellow peas, intake 80g (once a day) of yellow peas for 1 weeks

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

65 years-old >

Gender

Male and Female

Key inclusion criteria

1.Persons who received a sufficient explanation of the purpose and contents of the exam, have the capacity to consent, applied with free will with sufficient understanding, and agreed to participate
2.Adults who are 20 years old or more and under 65 years old
3.Persons who do not tend to take vinegar, natto or yellow peas
4.Persons who can eat vinegar, natto or yellow peas

Key exclusion criteria

1.Persons who have chronic illness, receiving medication, have a serious disease history
2.Persons who are allergic to the test food
3.Persons who usually take the test food
4.Persons who usually take medicine, specified health food, healthy food and supplements
5.Persons who have participated in other tests within the first month before the start of the test, or those who intend to participate in another exam after consenting to this exam
6.Persons who were judged as inappropriate for study participants by the principal investigator
7.Persons who are pregnant, planning or hoping to be pregnant during the study period, breastfeeding

Target sample size

16


Research contact person

Name of lead principal investigator

1st name Hirohito
Middle name
Last name Ishikawa

Organization

Healthcare Systems Co., Ltd.

Division name

Clinical Research Department

Zip code

105-0004

Address

Park Place Bld. 5F, 5-27-1, Shinbashi, Minato-ku, Tokyo, JAPAN

TEL

03-6809-2722

Email

ishikawa@hc-sys.jp


Public contact

Name of contact person

1st name Kousei
Middle name
Last name Nishikawa

Organization

Healthcare Systems Co., Ltd.

Division name

Clinical Research Department

Zip code

105-0004

Address

Park Place Bld. 5F, 5-27-1, Shinbashi, Minato-ku, Tokyo, JAPAN

TEL

03-6809-2722

Homepage URL


Email

nishikawa@hc-sys.jp


Sponsor or person

Institute

Healthcare Systems Co., Ltd.

Institute

Department

Personal name



Funding Source

Organization

Mizkan Holdings co.,ltd.

Organization

Division

Category of Funding Organization

Profit organization

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

The Ethics Committee of Healthcare Systems Co., Ltd.

Address

1-14-18, Shirakane, Showa-ku, Nagoya, Aichi, JAPAN

Tel

03-6809-2722

Email

soumu@hc-sys.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

2024 Year 11 Month 08 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

Preinitiation

Date of protocol fixation

2024 Year 11 Month 01 Day

Date of IRB


Anticipated trial start date

2024 Year 11 Month 08 Day

Last follow-up date

2025 Year 03 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2024 Year 11 Month 08 Day

Last modified on

2024 Year 11 Month 08 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000064104