UMIN-ICDS Clinical Trial

Unique ID issued by UMIN UMIN000049455
Receipt number R000056229
Scientific Title Evaluation test for improvement of intestinal environment by baby food containing a lot of vegetables
Date of disclosure of the study information 2023/01/01
Last modified on 2023/11/14 07:48:00

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Basic information

Public title

Evaluation test for improvement of intestinal environment by baby food containing a lot of vegetables

Acronym

Evaluation test for improvement of intestinal environment by baby food containing a lot of vegetables

Scientific Title

Evaluation test for improvement of intestinal environment by baby food containing a lot of vegetables

Scientific Title:Acronym

Evaluation test for improvement of intestinal environment by baby food containing a lot of vegetables

Region

Japan


Condition

Condition

healthy infants

Classification by specialty

Child

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

Investigate changes in body condition and intestinal microflora as a result of consumption of vegetable-rich baby food.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Physical condition by questionnaire Changes before and after(4 weeks intake)

Key secondary outcomes

Before and after comparison of intestinal microflora(4 weeks intake)


Base

Study type

Interventional


Study design

Basic design

Single arm

Randomization

Non-randomized

Randomization unit


Blinding

Open -no one is blinded

Control

Uncontrolled

Stratification

NO

Dynamic allocation

NO

Institution consideration

Institution is not considered as adjustment factor.

Blocking

NO

Concealment

No need to know


Intervention

No. of arms

1

Purpose of intervention

Prevention

Type of intervention

Food

Interventions/Control_1

Consume a selection of 10 test foods at least twice a day for 4 weeks

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

9 months-old <=

Age-upper limit

12 months-old >=

Gender

Male and Female

Key inclusion criteria

1. infants between 9 and 12 months of age
2. infants prone to constipation
3. infants who have obtained written consent from their parents or guardians
4. Healthy infants who are not receiving any medical treatment or medication
5. Infants who are able to maintain a regular daily routine during the study period.

Key exclusion criteria

1. Infants with possible food allergy to the test food
2. Infants who are deemed ineligible by the investigator to participate in this study.

Target sample size

30


Research contact person

Name of lead principal investigator

1st name Mamoru
Middle name
Last name Kimura

Organization

Kewpie Corporation

Division name

R&D Division

Zip code

182-0002

Address

2-5-7, Sengawa-cho, Chofu-shi,Tokyo,Japan

TEL

03-5384-7758

Email

mamoru_kimura@kewpie.co.jp


Public contact

Name of contact person

1st name Mamoru
Middle name
Last name Kimura

Organization

Kewpie Corporation

Division name

R&D Division

Zip code

182-0002

Address

2-5-7, Sengawa-cho, Chofu-shi,Tokyo,Japan

TEL

03-5384-7758

Homepage URL


Email

mamoru_kimura@kewpie.co.jp


Sponsor or person

Institute

Kewpie Corporation

Institute

Department

Personal name



Funding Source

Organization

Kewpie Corporation

Organization

Division

Category of Funding Organization

Profit organization

Nationality of Funding Organization

Japan


Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Ueno Asagao Clinic Ethics Review Board

Address

Kairaku Building 6F,2-7-5, Ueno, Taito-ku,Tokyo,Japan

Tel

03-6801-8480

Email

t.tamura@tes-h.co.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 01 Month 01 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

19

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 10 Month 17 Day

Date of IRB

2022 Year 10 Month 19 Day

Anticipated trial start date

2022 Year 11 Month 10 Day

Last follow-up date

2023 Year 02 Month 28 Day

Date of closure to data entry

2023 Year 06 Month 15 Day

Date trial data considered complete

2023 Year 06 Month 15 Day

Date analysis concluded

2023 Year 06 Month 15 Day


Other

Other related information



Management information

Registered date

2022 Year 11 Month 08 Day

Last modified on

2023 Year 11 Month 14 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/icdr_e/ctr_view.cgi?recptno=R000056229


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name