UMIN-CTR Clinical Trial

Basic information
Public title	Effect on skin condition by using in combination composite facial equipment with cosmetic lotion
Acronym	DWHP study
Scientific Title	Effect on skin condition by using in combination composite facial equipment with cosmetic lotion: single blinded study
Scientific Title:Acronym	Effect on skin condition by using in combination composite facial equipment with cosmetic lotion
Region	Japan

Condition
Condition	Healthy adult Female
Classification by specialty	Adult
Classification by malignancy	Others
Genomic information	NO

Objectives
Narrative objectives1	Compare the effects of using a composite facial equipment with cosmetic lotion on skin condition
Basic objectives2	Efficacy
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase

Assessment
Primary outcomes	skin condition measurement(before use, immediately after use, 4 weeks later)
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	Active
Stratification
Dynamic allocation
Institution consideration
Blocking
Concealment

Intervention
No. of arms	2
Purpose of intervention	Treatment
Type of intervention	Device,equipment Other
Interventions/Control_1	Use 2 items of test articles (facial equipment, 2 types of cosmetic lotion) on one side of the face for 4 weeks
Interventions/Control_2	Use 2 types of cosmetic lotion on the other side for 4 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	55 years-old >=
Gender	Female
Key inclusion criteria	1.Subjects whose wrinkle class in the outer corner of eye is 1 to 3 2.Subjects who want to care for sagging face, sagging cheeks, and sagging chin 3. Subjects with dry skin
Key exclusion criteria	1. Subjects with cosmetic allergy or metal allergy 2. Subjects who are pregnant or breastfeeding 3. Subjects who have inflammation or wound on their face 4. Subjects with sensitive skin 5. Subjects who are judged as unsuitable for the study by the investigator for the other reason
Target sample size	16

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
Institute	Japan Clinical Trial Association
Institute
Department

Funding Source
Organization	YA-MAN 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	2022 Year 01 Month 17 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	15
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	2021 Year 12 Month 03 Day
Date of IRB	2022 Year 01 Month 06 Day
Anticipated trial start date	2022 Year 01 Month 17 Day
Last follow-up date	2022 Year 02 Month 15 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 01 Month 13 Day
Last modified on	2022 Year 05 Month 13 Day

Link to view the page
URL(English)	https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000053189

Research Plan
Registered date	File name

Research case data specifications
Registered date	File name

Research case data
Registered date	File name

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