UMIN-ICDS Clinical Trial

Unique ID issued by UMIN UMIN000048632
Receipt number R000055417
Scientific Title Evaluation of the efficacy and safety of topical cream on the properties of normal human stratum corneum: An exploratory study.
Date of disclosure of the study information 2022/10/10
Last modified on 2022/08/09 14:17:42

* This page includes information on clinical trials registered in UMIN clinical trial registed system.
* We don't aim to advertise certain products or treatments


Basic information

Public title

Evaluation of the efficacy and safety of topically applied cream on the properties of human stratum corneum.

Acronym

Evaluation of the efficacy and safety of topically applied cream on the properties of human stratum corneum.

Scientific Title

Evaluation of the efficacy and safety of topical cream on the properties of normal human stratum corneum: An exploratory study.

Scientific Title:Acronym

Evaluation of the efficacy and safety of topical cream on the properties of normal human stratum corneum: An exploratory study.

Region

Japan


Condition

Condition

Healthy adult male

Classification by specialty

Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

The effect of cream applied topically twice a day for 4 weeks on the improvement of human stratum corneum properties and safety will be exploratively investigated.

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Skin color (Lab)
Water content of stratum corneum
Transepidermal water loss
Stratum corneum collection
Skin observation by doctor

Key secondary outcomes



Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit

Individual

Blinding

Open -but assessor(s) are blinded

Control

No treatment

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

2

Purpose of intervention

Prevention

Type of intervention

Other

Interventions/Control_1

The test product, which is dispensed with two pushes, will be applied topically twice a day for 4 weeks.

Interventions/Control_2

Un treated

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

25 years-old <=

Age-upper limit

60 years-old >

Gender

Male

Key inclusion criteria

- Healthy adult males between the ages of 25 and 60 years old.
- Subjects who can undergo the designated tests within the study period.

Key exclusion criteria

- Subjects with chronic physical diseases such as diabetes, heart disease, kidney disease or liver dysfunction.
- Subjects who have demonstrated a previous hypersensitivity reaction to any of the cosmetic products.
- Subjects who have demonstrated a previous hypersensitivity reaction to adhesive tapes, medical tapes, or rubber.
- Subjects with skin disease such as atopic dermatitis.
- Subjects who have scars, nevus pimentosus, acne, erythema, or telangiectasia at the test sites.
- Subjects who have undergone the plastic surgery at the test sites.
- Subjects with excessively tanned skin at the test sites.
- Subjects who have shaved, epilated, or removed hair from the test sites. for at least one month prior to obtaining consent.
- Subjects who have topically applied drugs regularly at the test sites for at least one month prior to obtaining consent.
- Subjects who have habitually washed their own skin with nylon or other solid materials for at least one month prior to obtaining consent.
- Subjects who have undergone aesthetic plastic surgery such as peeling or laser irradiation at the test sites for at least six months prior to obtaining consent.
- Subjects who are scheduled to receive vaccinations within the study period.
- Subjects who are judged by doctor to be inappropriate for this study.

Target sample size

10


Research contact person

Name of lead principal investigator

1st name Syota
Middle name
Last name Shimizu

Organization

Otsuka Pharmaceutical Co., Ltd.

Division name

Otsu Skin Care Research Institute

Zip code

520-0002

Address

3-31-13 Saigawa, Otsu, Shiga, Japan

TEL

077-521-8835

Email

Shimizu.Syota@otsuka.jp


Public contact

Name of contact person

1st name Syota
Middle name
Last name Shimizu

Organization

Otsuka Pharmaceutical Co., Ltd.

Division name

Otsu Skin Care Research Institute

Zip code

520-0002

Address

3-31-13 Saigawa, Otsu, Shiga, Japan

TEL

077-521-8835

Homepage URL


Email

Shimizu.Syota@otsuka.jp


Sponsor or person

Institute

Otsuka Pharmaceutical Co., Ltd.

Institute

Department

Personal name



Funding Source

Organization

none

Organization

Division

Category of Funding Organization

Self funding

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Otsuka Pharmaceutical Co., Ltd.

Address

Shinagawa Grand Central Tower, 2-16-4, Konan, Minato-ku, Tokyo

Tel

03-6717-1499

Email

shimizu_se@otsuka.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

2022 Year 10 Month 10 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

8

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 05 Month 09 Day

Date of IRB

2022 Year 05 Month 11 Day

Anticipated trial start date

2022 Year 05 Month 20 Day

Last follow-up date

2022 Year 07 Month 07 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2022 Year 08 Month 09 Day

Last modified on

2022 Year 08 Month 09 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/icdr_e/ctr_view.cgi?recptno=R000055417


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name