UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000052550 |
|---|---|
| Receipt number | R000059961 |
| Scientific Title | Comprehensive evaluation of skin condition when using facial beauty device equipped with high brightness LED and low output IPL together with beauty serum: single blinded study |
| Date of disclosure of the study information | 2023/10/20 |
| Last modified on | 2024/03/22 09:50:07 |
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Basic information
Public title
Comprehensive evaluation of skin condition when using facial beauty device equipped with high brightness LED and low output IPL together with beauty serum
Acronym
BGS study
Scientific Title
Comprehensive evaluation of skin condition when using facial beauty device equipped with high brightness LED and low output IPL together with beauty serum: single blinded study
Scientific Title:Acronym
Comprehensive evaluation of skin condition when using facial beauty device equipped with high brightness LED and low output IPL together with beauty serum
Region
| Japan |
Condition
Condition
Healthy adult Female
Classification by specialty
| Adult |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
Effects on skin condition by using facial device and cosmetics in combination
Basic objectives2
Efficacy
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
Evaluation of devices that measure (before use, after 4 weeks, after 8 weeks, after 12 weeks)
Key secondary outcomes
subjective assessment
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 device, cosmetic serum) on one side of the face for 12 weeks
Interventions/Control_2
Use cosmetic serum on the other side 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
| 35 | years-old | <= |
Age-upper limit
| 59 | years-old | >= |
Gender
Female
Key inclusion criteria
1) Subjects with dull skin
2) Subjects with disturbed skin texture, Subjects with rough skin texture
3) Subjects whose makeup doesn't apply well
4) Subjects who have not had excessive sunburn within the past 4 weeks
5) Subjects of dry skin
Key exclusion criteria
1.Those who are pregnant or may be pregnant, and those who are breastfeeding
2.Persons who work night shifts or day and night shifts
3.Individuals who need help from others and are unable to walk independently.
4.Subjects participating in other clinical trials
5.Factors that may affect the test results (disease such as atopic dermatitis and urticaria, inflammation, eczema, trauma, acne, tumor warts with a diameter of 5 cm or more on the cheek, etc.) , or traces of it)
6.Subjects who are judged as unsuitable for the study by the investigator for the other reason
Target sample size
12
Research contact person
Name of lead principal investigator
| 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
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
info@yakujihou.org
Sponsor or person
Institute
Japan Clinical Trial Association
Institute
Department
Personal name
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
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
| 2023 | Year | 10 | Month | 20 | 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
17
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
| 2023 | Year | 09 | Month | 05 | Day |
Date of IRB
| 2023 | Year | 09 | Month | 14 | Day |
Anticipated trial start date
| 2023 | Year | 10 | Month | 20 | Day |
Last follow-up date
| 2024 | Year | 01 | Month | 12 | 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 | 10 | Month | 19 | Day |
Last modified on
| 2024 | Year | 03 | Month | 22 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000059961
