UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000036715 |
|---|---|
| Receipt number | R000041835 |
| Scientific Title | blood sampling from the patients recovered from serious diseases(Yamakagashi bites, Red back spider bites, diphtheria, gas gangrene, and botulinus) |
| Date of disclosure of the study information | 2019/05/15 |
| Last modified on | 2019/05/11 23:50:38 |
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Basic information
Public title
blood sampling from the patients recovered from serious diseases(Yamakagashi bites, Red back spider bites, diphtheria, gas gangrene, and botulinus)
Acronym
blood sampling from the patients recovered from serious diseases(Yamakagashi bites, Red back spider bites, diphtheria, gas gangrene, and botulinus)
Scientific Title
blood sampling from the patients recovered from serious diseases(Yamakagashi bites, Red back spider bites, diphtheria, gas gangrene, and botulinus)
Scientific Title:Acronym
blood sampling from the patients recovered from serious diseases(Yamakagashi bites, Red back spider bites, diphtheria, gas gangrene, and botulinus)
Region
| Japan |
Condition
Condition
Yamakagashi bites, Red back spider bites, diphtheria, gas gangrene, and botulinus
Classification by specialty
| Infectious disease | Emergency medicine | Intensive care medicine |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
To produce monoclonal antitoxin for Yamakagashi bites, Red back spider bites, diphtheria, gas gangrene, and botulinus
Basic objectives2
Others
Basic objectives -Others
None
Trial characteristics_1
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
None
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
Treatment
Type of intervention
| Vaccine |
Interventions/Control_1
None
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
| 6 | years-old | <= |
Age-upper limit
| 90 | years-old | > |
Gender
Male and Female
Key inclusion criteria
Patients recovered from serious diseases
Key exclusion criteria
Pregnant women
Infants
Target sample size
10
Research contact person
Name of lead principal investigator
| 1st name | Toru |
| Middle name | |
| Last name | Hifumi |
Organization
St. Luke's International Hospital
Division name
Emergency Medicine
Zip code
104-8560
Address
9-1, Akashicho, Chuouku,Tokyo
TEL
03-3541-5151
hifumitoru@gmail.com
Public contact
Name of contact person
| 1st name | Toru |
| Middle name | |
| Last name | Hifumi |
Organization
St. Luke's International Hospital
Division name
Emergency Medicine
Zip code
104-8560
Address
9-1, Akashicho, Chuouku,Tokyo
TEL
03-3541-5151
Homepage URL
hifumitoru@gmail.com
Sponsor or person
Institute
St. Luke's International Hospital
Institute
Department
Personal name
Funding Source
Organization
AMED
Organization
Division
Category of Funding Organization
Japanese Governmental office
Nationality of Funding Organization
Other related organizations
Co-sponsor
Name of secondary funder(s)
IRB Contact (For public release)
Organization
St. Luke's International Hospital
Address
9-1, Akashicho, Chuouku,Tokyo
Tel
03-3541-5151
hifumitoru@gmail.com
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
| 2019 | Year | 05 | Month | 15 | 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
Preinitiation
Date of protocol fixation
| 2019 | Year | 05 | Month | 10 | Day |
Date of IRB
Anticipated trial start date
| 2019 | Year | 05 | Month | 15 | 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
Management information
Registered date
| 2019 | Year | 05 | Month | 11 | Day |
Last modified on
| 2019 | Year | 05 | Month | 11 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000041835
