UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000040461
Receipt number R000046186
Scientific Title Effect of skin condition (excretion of melanin pigment, epidermal turnover) of combined use of medicated cosmetic and massage with specific method : single blinded study
Date of disclosure of the study information 2020/05/27
Last modified on 2020/11/18 10:03:07

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Basic information

Public title

Effect of skin condition (excretion of melanin pigment, epidermal turnover) of combined use of medicated cosmetic and massage with specific method

Acronym

SMS turnover trial

Scientific Title

Effect of skin condition (excretion of melanin pigment, epidermal turnover) of combined use of medicated cosmetic and massage with specific method : single blinded study

Scientific Title:Acronym

Effect of skin condition (excretion of melanin pigment, epidermal turnover) of combined use of medicated cosmetic and massage with specific method

Region

Japan


Condition

Condition

Healthy adult

Classification by specialty

Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

Evaluate the skin condition (excretion of melanin pigment, epidermal turnover) after using medicated cosmetic and massage with specific method for 12 weeks

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

equipment evaluation, visual evaluation, subjective evaluation

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

Treatment

Type of intervention

Other

Interventions/Control_1

Run the test program for 12 weeks

Interventions/Control_2

Regular skin care for 8 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

35 years-old <=

Age-upper limit

59 years-old >=

Gender

Male and Female

Key inclusion criteria

Subjects with pigmentation on the face

Key exclusion criteria

1. Subjects with cosmetic allergies
2. Subjects who are pregnant or lactating
3. Subjects with inflamed or scraped skin on face
4. Subjects who are taking medicine for pigmentation, those who are treating pigmentation
5. Subjects who are judged as unsuitable for the study by the investigator for the other reason

Target sample size

30


Research contact person

Name of lead principal investigator

1st name Masatomo
Middle name
Last name Najima

Organization

Japan Clinical Trial Association

Division name

N.A.

Zip code

1600022

Address

5F, 4-3-17 Shinjuku, Shinjukuku, Tokyo

TEL

0364574666

Email

info@yakujihou.org


Public contact

Name of contact person

1st name Takeshi
Middle name
Last name Kaneko

Organization

Japan Clinical Trial Association

Division name

N.A.

Zip code

1600022

Address

5F, 4-3-17 Shinjuku, Shinjukuku, Tokyo

TEL

0364574666

Homepage URL


Email

info@yakujihou.org


Sponsor or person

Institute

Japan Clinical Trial Association

Institute

Department

Personal name



Funding Source

Organization

Mebius Pharmaceutical Co.,Ltd.

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

Institutional Review Board of Pharmaceutical Law Wisdoms

Address

5F, 4-3-17 Shinjuku, Shinjukuku, Tokyo

Tel

0364574911

Email

master@yakujihou.net


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

2020 Year 05 Month 27 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

28

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

2020 Year 04 Month 16 Day

Date of IRB

2020 Year 04 Month 23 Day

Anticipated trial start date

2020 Year 05 Month 27 Day

Last follow-up date

2020 Year 08 Month 20 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2020 Year 05 Month 20 Day

Last modified on

2020 Year 11 Month 18 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000046186


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name