UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000026329 |
|---|---|
| Receipt number | R000030243 |
| Scientific Title | Clinical evaluation of wrinkle improvement by cosmetics |
| Date of disclosure of the study information | 2017/03/02 |
| Last modified on | 2017/06/19 11:11:35 |
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Basic information
Public title
Clinical evaluation of wrinkle improvement by cosmetics
Acronym
Clinical evaluation of wrinkle improvement by cosmetics
Scientific Title
Clinical evaluation of wrinkle improvement by cosmetics
Scientific Title:Acronym
Clinical evaluation of wrinkle improvement by cosmetics
Region
| Japan |
Condition
Condition
Not applicable
Classification by specialty
| Dermatology | Adult |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
The objective of this study is to reveal that the test cosmetics can reduce eye area wrinkles caused by dryness
Basic objectives2
Efficacy
Basic objectives -Others
Trial characteristics_1
Confirmatory
Trial characteristics_2
Pragmatic
Developmental phase
Not applicable
Assessment
Primary outcomes
The wrinkle depth evaluated using replica of eye area
Key secondary outcomes
The wrinkle grade evaluated using a picture of eye area
Base
Study type
Interventional
Study design
Basic design
Factorial
Randomization
Randomized
Randomization unit
Cluster
Blinding
Single blind -investigator(s) and assessor(s) are blinded
Control
No treatment
Stratification
Dynamic allocation
Institution consideration
Blocking
Concealment
No need to know
Intervention
No. of arms
2
Purpose of intervention
Treatment
Type of intervention
| Other |
Interventions/Control_1
Application of the test cosmetics A in one eye area for 4 weeks.
No application of the test cosmetics in another eye area for 4 weeks.
Interventions/Control_2
Application of the test cosmetics B in one eye area for 4 weeks.
No application of the test cosmetics in another eye area 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
| Not applicable |
Gender
Female
Key inclusion criteria
(1)A person who has 1 to 3 wrincle grade in eye area.
(2)A Japanese woman over 30 years old(when a written informed consent was obtained)
(3)A person who consented to participate in this study in the document
Key exclusion criteria
(1)A person who varies in wrinkle grade on the left and right
(2)A person who has factors influencing the test at the evaluation site (those with atopic dermatitis and the like, trauma, burns, inflammation, acne, warts or traces thereof)
(3)A person who has history of beauty care that influence the test at the evaluation site, or those who plans to receive it during the study period
(4)A person who received special treatment (facial esthetics etc.) at the evaluation site within the past 3 months, or who will receive it during the study period
(5)Pregnant or lactating
(6)A person who has experienced severe disease (allergy, etc.) against cosmetics
(7)A person who continues to use cosmetics, health foods, etc. that indicate or appeal the efficacy related to this study to the evaluation site
(8)A person judged as ineligible by the investigator with other reasons
Target sample size
30
Research contact person
Name of lead principal investigator
| 1st name | |
| Middle name | |
| Last name | Kazuhiko Takano |
Organization
Medical Corporation Hokubukai Utsukushigaoka Hospital
Division name
Center for Clinical Pharmacology
Zip code
Address
61-1, Sinei, Kiyota-ku, Sapporo, Hokkaido, Japan
TEL
011-882-0111
wakimoto@ughp-cpc.jp
Public contact
Name of contact person
| 1st name | |
| Middle name | |
| Last name | Ryota Wakimoto |
Organization
Medical Corporation Hokubukai Utsukushigaoka Hospital
Division name
Center for Clinical Pharmacology
Zip code
Address
61-1, Sinei, Kiyota-ku, Sapporo, Hokkaido, Japan
TEL
011-882-0111
Homepage URL
wakimoto@ughp-cpc.jp
Sponsor or person
Institute
Medical Corporation Hokubukai Utsukushigaoka Hospital
Institute
Department
Personal name
Funding Source
Organization
Noevir Co., Ltd.
Organization
Division
Category of Funding Organization
Profit organization
Nationality of Funding Organization
Japan
Other related organizations
Co-sponsor
Name of secondary funder(s)
IRB Contact (For public release)
Organization
Address
Tel
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
医療法人北武会 美しが丘病院（北海道） Medical Corporation Hokubukai Utsukushigaoka Hospital
Other administrative information
Date of disclosure of the study information
| 2017 | Year | 03 | Month | 02 | 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 | 02 | Month | 16 | Day |
Date of IRB
Anticipated trial start date
| 2017 | Year | 03 | Month | 02 | Day |
Last follow-up date
Date of closure to data entry
Date trial data considered complete
Date analysis concluded
Other
Other related information
Management information
Registered date
| 2017 | Year | 02 | Month | 28 | Day |
Last modified on
| 2017 | Year | 06 | Month | 19 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000030243
