UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000027457
Receipt number R000031455
Scientific Title A study on noninvasive in vivo analysis of human skin
Date of disclosure of the study information 2017/05/26
Last modified on 2021/05/24 12:33:03

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Basic information

Public title

A study on noninvasive in vivo analysis of human skin

Acronym

A study on noninvasive in vivo analysis of human skin

Scientific Title

A study on noninvasive in vivo analysis of human skin

Scientific Title:Acronym

A study on noninvasive in vivo analysis of human skin

Region

Japan


Condition

Condition

Healthy adults

Classification by specialty

Dermatology Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To confirm the relationship between noninvasive in vivo analysis and dermatological conditions for healthy female skin

Basic objectives2

Others

Basic objectives -Others

Observational study

Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Evaluation of wrinkle formation, skin water content, transepidermal water loss, skin elasticity and OCT.

Key secondary outcomes



Base

Study type

Interventional


Study design

Basic design

Single arm

Randomization

Non-randomized

Randomization unit


Blinding

Open -no one is blinded

Control

Uncontrolled

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

1

Purpose of intervention

Prevention

Type of intervention

Other

Interventions/Control_1

Measurement in constant temperature and humidity room.

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

Female

Key inclusion criteria

Healthy Japanese females

Key exclusion criteria

-Subjects with sensitive skin or allergy against facial cleanser or cosmetic products
-Subjects with skin diseases such as atopic dermatitis, psoriasis and severe acne
-Subjects with pollen allergy
-Subjects seemed inappropriate to participate in this study by the principle investigator
-Subjects who have medical treatment or take some medicine for their facial skin

Target sample size

44


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Tetsuya Sayou

Organization

Kao Corporation

Division name

R&D -Core Technology- Biological Science Research

Zip code


Address

3-28, 5-chome, Kotobuki-cho, Odawara, Kanagawa, 250-0002, JAPAN

TEL

+81-465-34-6116

Email

sayou.tetsuya@kao.co.jp


Public contact

Name of contact person

1st name
Middle name
Last name Kohei Yamazaki

Organization

Kao Corporation

Division name

R&D -Core Technology- Biological Science Research

Zip code


Address

3-28, 5-chome, Kotobuki-cho, Odawara, Kanagawa, 250-0002, JAPAN

TEL

+81-465-34-6116

Homepage URL


Email

yamazaki.kouhei@kao.co.jp


Sponsor or person

Institute

Kao Corporation

Institute

Department

Personal name



Funding Source

Organization

Kao Corporation

Organization

Division

Category of Funding Organization

Profit organization

Nationality of Funding Organization



Other related organizations

Co-sponsor

University of Tsukuba

Name of secondary funder(s)



IRB Contact (For public release)

Organization


Address


Tel


Email



Secondary IDs

Secondary IDs

YES

Study ID_1

H29-A023

Org. issuing International ID_1

701 Research, Inc

Study ID_2


Org. issuing International ID_2


IND to MHLW



Institutions

Institutions

株式会社セブンオーワンリサーチ Above Access(東京)
国立大学法人筑波大学(茨城)


Other administrative information

Date of disclosure of the study information

2017 Year 05 Month 26 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

Completed

Date of protocol fixation

2017 Year 05 Month 18 Day

Date of IRB

2017 Year 05 Month 18 Day

Anticipated trial start date

2017 Year 06 Month 06 Day

Last follow-up date

2021 Year 05 Month 21 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2017 Year 05 Month 23 Day

Last modified on

2021 Year 05 Month 24 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000031455


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name