UMIN-ICDS Clinical Trial

Unique ID issued by UMIN UMIN000051826
Receipt number R000059144
Scientific Title Study of the effects of food ingredients on skin elasticity
Date of disclosure of the study information 2023/08/21
Last modified on 2024/02/04 09:58:10

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Basic information

Public title

Study of the effects of food ingredients on skin elasticity (SWE-2023-06- HCRINK)

Acronym

Study of the effects of food ingredients on skin elasticity

Scientific Title

Study of the effects of food ingredients on skin elasticity

Scientific Title:Acronym

Study of the effects of food ingredients on skin elasticity

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

Basic objectives2

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, Japan.

TEL

050-3182-0568

Email

Hidenori_Obata@suntory.co.jp


Public contact

Name of contact person

1st name Keisuke
Middle name
Last name Yasumoto

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, Japan.

TEL

050-3182-0496

Homepage URL


Email

Keisuke_Yasumoto@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, JAPAN

Tel

03-6240-1162

Email

jimukyoku@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 08 Month 21 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

140

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

No longer recruiting

Date of protocol fixation

2023 Year 08 Month 02 Day

Date of IRB

2023 Year 07 Month 27 Day

Anticipated trial start date

2023 Year 09 Month 13 Day

Last follow-up date

2023 Year 12 Month 18 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 08 Month 04 Day

Last modified on

2024 Year 02 Month 04 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/icdr_e/ctr_view.cgi?recptno=R000059144


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name