UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000013052 |
|---|---|
| Receipt number | R000015183 |
| Scientific Title | Clinical study using samples of patients experienced systemic side effects by vaccines |
| Date of disclosure of the study information | 2014/02/03 |
| Last modified on | 2019/08/16 11:52:50 |
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Basic information
Public title
Clinical study using samples of patients experienced systemic side effects by vaccines
Acronym
Clinical study using samples of patients experienced systemic side effects by vaccines
Scientific Title
Clinical study using samples of patients experienced systemic side effects by vaccines
Scientific Title:Acronym
Clinical study using samples of patients experienced systemic side effects by vaccines
Region
| Japan |
Condition
Condition
systemic side effects by vaccines
Classification by specialty
| Clinical immunology | Infectious disease |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
Objectives of this study are to search the mechanism of side effect related vaccines.
Basic objectives2
Safety
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
This study measures microRNA and mRNA by chip analysis, and also measures antibodies, cytokines and chemokines by ELISA.
Key secondary outcomes
Base
Study type
Observational
Study design
Basic design
Randomization
Randomization unit
Blinding
Control
Stratification
Dynamic allocation
Institution consideration
Blocking
Concealment
Intervention
No. of arms
Purpose of intervention
Type of intervention
Interventions/Control_1
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
| Not applicable |
Age-upper limit
| Not applicable |
Gender
Male and Female
Key inclusion criteria
Those who are experienced systemic side effect of vaccine, and who agree to participate this study
Key exclusion criteria
Not obtained the consent
Target sample size
2
Research contact person
Name of lead principal investigator
| 1st name | |
| Middle name | |
| Last name | Ken Ishii |
Organization
National Institutes of Biomedical Innovation,Health and Nutrition
Division name
Laboratory of Adjuvant Innovation
Zip code
Address
7-6-8 Asagi Saito Ibaraki-City Osaka
TEL
072-641-8043
kenishii@biken.osaka-u.ac.jp
Public contact
Name of contact person
| 1st name | |
| Middle name | |
| Last name | Ken Ishii |
Organization
National Institutes of Biomedical Innovation,Health and Nutrition
Division name
Laboratory of Adjuvant Innovation
Zip code
Address
7-6-8 Asagi Saito Ibaraki-City Osaka
TEL
072-641-8043
Homepage URL
kenishii@biken.osaka-u.ac.jp
Sponsor or person
Institute
National Institutes of Biomedical Innovation,Health and Nutrition
Institute
Department
Personal name
Funding Source
Organization
Japan Agency for Medical Research and Development
Organization
Division
Category of Funding Organization
Other
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
| 2014 | Year | 02 | Month | 03 | 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 | 07 | Month | 24 | Day |
Date of IRB
| 2013 | Year | 08 | Month | 02 | Day |
Anticipated trial start date
| 2013 | Year | 10 | Month | 01 | Day |
Last follow-up date
| 2022 | Year | 03 | Month | 31 | Day |
Date of closure to data entry
Date trial data considered complete
Date analysis concluded
Other
Other related information
sample
Serum, plasma, cerebrospinal fluid, biopsy tissue sample
analysis
Analyze between clinical information including which kind of vaccine, and obtained dates of samples
Management information
Registered date
| 2014 | Year | 02 | Month | 03 | Day |
Last modified on
| 2019 | Year | 08 | Month | 16 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000015183
