UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000011199 |
|---|---|
| Receipt number | R000013053 |
| Scientific Title | Study of skin properties of children for intradermal vaccine administration |
| Date of disclosure of the study information | 2013/07/17 |
| Last modified on | 2014/01/16 16:36:23 |
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Basic information
Public title
Study of skin properties of children for intradermal vaccine administration
Acronym
Study of skin properties of children for intradermal vaccine administration
Scientific Title
Study of skin properties of children for intradermal vaccine administration
Scientific Title:Acronym
Study of skin properties of children for intradermal vaccine administration
Region
| Japan |
Condition
Condition
Healty
Classification by specialty
| Pediatrics |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
Evaluate skin properties including it thickness of 13-15 year-old children.
Basic objectives2
Others
Basic objectives -Others
property analysis
Trial characteristics_1
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
Skin cross section image examination(skin thickness)
Skin property (hardness, elasticity, viscosity)
Key secondary outcomes
Base
Study type
Interventional
Study design
Basic design
Single arm
Randomization
Non-randomized
Randomization unit
Blinding
Open -no one is blinded
Control
Uncontrolled
Stratification
Dynamic allocation
Institution consideration
Blocking
Concealment
Intervention
No. of arms
1
Purpose of intervention
Prevention
Type of intervention
| Device,equipment |
Interventions/Control_1
Ultrasound echography
Skin property sensing
Interventions/Control_2
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
| 13 | years-old | <= |
Age-upper limit
| 15 | years-old | >= |
Gender
Male and Female
Key inclusion criteria
-Japanese
-A person 13-15 years of age
-a person without skin disease or any other histories infecting condition of skin
-Those who written informed consent is obtained from
-Healthy person
Key exclusion criteria
-A person who has any abnormality in the application site.
-A person who are deemed to have high risk to ultra-sound imaging examination.
-Those who are deemed inappropriate to participate in this study by doctor.
Target sample size
80
Research contact person
Name of lead principal investigator
| 1st name | |
| Middle name | |
| Last name | Masaaki Mori |
Organization
Yokohama City University Medical Center
Division name
Department of Pediatrics
Zip code
Address
4-57 Urafune-cho, Minami-ku, yokohama 232-0024, Japan
TEL
+81-45-261-5656
mmorii@med.yokohama-cu.ac.jp
Public contact
Name of contact person
| 1st name | |
| Middle name | |
| Last name | Takuma Hara |
Organization
Yokohama City University Medical Center
Division name
Department of Pediatrics
Zip code
Address
4-57 Urafune-cho, Minami-ku, yokohama 232-0024, Japan
TEL
+81-45-261-5656
Homepage URL
mmorii@med.yokohama-cu.ac.jp
Sponsor or person
Institute
Yokohama City Univ, Medical Center
Institute
Department
Personal name
Funding Source
Organization
TERUMO CORPORATION
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
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
Other administrative information
Date of disclosure of the study information
| 2013 | Year | 07 | 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
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
| 2013 | Year | 05 | Month | 23 | Day |
Date of IRB
Anticipated trial start date
| 2013 | Year | 07 | Month | 01 | 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
| 2013 | Year | 07 | Month | 16 | Day |
Last modified on
| 2014 | Year | 01 | Month | 16 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000013053
