UMIN-ICDS Clinical Trial

Unique ID issued by UMIN UMIN000053109
Receipt number R000060609
Scientific Title Study of the effects of ingestion of food components on skin elasticity and safety evaluation of long-term ingestion
Date of disclosure of the study information 2024/01/09
Last modified on 2023/12/14 21:14:29

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Basic information

Public title

Study of the effects of ingestion of food components on skin elasticity and safety evaluation of long-term ingestion (SWE-2023-08- HCRINK)

Acronym

Study of the effects of ingestion of food components on skin elasticity and safety evaluation of long-term ingestion

Scientific Title

Study of the effects of ingestion of food components on skin elasticity and safety evaluation of long-term ingestion

Scientific Title:Acronym

Study of the effects of ingestion of food components on skin elasticity and safety evaluation of long-term ingestion

Region

Japan


Condition

Condition

Not applicable

Classification by specialty

Not applicable Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To evaluate the effects of food ingredients on skin elasticity and safety of long-term ingestion

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Skin viscoelasticity

Key secondary outcomes



Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit

Individual

Blinding

Double blind -all involved are blinded

Control

Placebo

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

2

Purpose of intervention

Prevention

Type of intervention

Food

Interventions/Control_1

Intake of the test foods for 12 weeks.

Interventions/Control_2

Intake of the control foods for 12 weeks.

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

30 years-old <=

Age-upper limit

64 years-old >=

Gender

Female

Key inclusion criteria

1) Healthy women aged 30 to 64 years.
2) Subjects who can come to the designated premises on the date of the scheduled visit.
3) Subjects who can understand the purpose and content of this study and agree in writing to participate in this study.

Key exclusion criteria

1) Subjects who keep irregular hours such as shift work.
2) Use of products affecting the data of this study, such as food for specified health use, food with function claims, and medicine.
3) Presence of previous and present diseases such as atopic dermatitis, cardiovascular diseases, diabetes and food allergy diseases.
4) Subjects with wounds or inflammation at the assessment site.
5) Subjects who have undergone surgery on the assessed site within the past year.
6) Subjects who routinely engage in tanning activities.
7) Investigator's judgment for other reason.

Target sample size

140


Research contact person

Name of lead principal investigator

1st name Hidenori
Middle name
Last name Obata

Organization

Suntory Wellness Limited

Division name

Institute For Science of Life

Zip code

619-0284

Address

8-1-1 Seikadai, Seika-cho, Soraku-gun, Kyoto. 619-0284, Japan.

TEL

050-3182-0568

Email

Hidenori_Obata@suntory.co.jp


Public contact

Name of contact person

1st name Mui
Middle name
Last name Iida

Organization

Suntory Wellness Limited

Division name

Institute For Science of Life

Zip code

619-0284

Address

8-1-1 Seikadai, Seika-cho, Soraku-gun, Kyoto. 619-0284, Japan.

TEL

050-1734-9361

Homepage URL


Email

Mui_Iida@suntory.co.jp


Sponsor or person

Institute

Suntory Wellness Limited

Institute

Department

Personal name



Funding Source

Organization

Suntory Wellness Limited

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

Ueno-Asagao Clinic Ethical Review Committee

Address

6F Kairaku Building 2-7-5 Higashiueno Taito-ku Tokyo 110-0015, JAPAN

Tel

03-6240-1162

Email

info@ueno-asagao.clinic


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 01 Month 09 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

2023 Year 12 Month 14 Day

Date of IRB

2023 Year 12 Month 13 Day

Anticipated trial start date

2024 Year 01 Month 10 Day

Last follow-up date

2024 Year 04 Month 26 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2023 Year 12 Month 14 Day

Last modified on

2023 Year 12 Month 14 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/icdr_e/ctr_view.cgi?recptno=R000060609


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name