UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000022937 |
|---|---|
| Receipt number | R000026422 |
| Scientific Title | Examination of the correlation of the histamine H3 receptor density and the neurocognitive function |
| Date of disclosure of the study information | 2016/06/30 |
| Last modified on | 2018/07/02 16:07:51 |
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Basic information
Public title
Examination of the correlation of the histamine H3 receptor density and the neurocognitive function
Acronym
Examination of the correlation of the histamine H3 receptor density and the neurocognitive function
Scientific Title
Examination of the correlation of the histamine H3 receptor density and the neurocognitive function
Scientific Title:Acronym
Examination of the correlation of the histamine H3 receptor density and the neurocognitive function
Region
| Japan |
Condition
Condition
Healthy volunteers
Classification by specialty
| Adult |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
Examination of the correlation of the histamine H3 receptor density and the neurocognitive functions in human brain.
Basic objectives2
Bio-availability
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
The correlation between the change of BOLD signals, the psychological changes and the histamine H3 receptor density.
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
Diagnosis
Type of intervention
| Medicine |
Interventions/Control_1
Day1
Medical examination (30min)
MRI scan (100min)
Psychological test (120min)
Day2
Medical examination (30min)
Psychological test (90min)
PET scan (150min)
Medical examination (30min)
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
| 20 | years-old | <= |
Age-upper limit
| 40 | years-old | > |
Gender
Male
Key inclusion criteria
Healthy individuals who have the ability to provide informed consent.
Key exclusion criteria
Psychiatric disorders including drug dependence
Serious medical illness
Target sample size
10
Research contact person
Name of lead principal investigator
| 1st name | |
| Middle name | |
| Last name | Takehito Ito |
Organization
National Institute of Radiological Sciences
Division name
Department of Functional Brain Imaging Research
Zip code
Address
4-9-1 Anagawa, Inage-ku, Chiba, Chiba 263-8555, Japan
TEL
043-206-3251
ito.takehito@qst.go.jp
Public contact
Name of contact person
| 1st name | |
| Middle name | |
| Last name | Kazuko Suzuki |
Organization
National Institute of Radiological Sciences
Division name
Clinical Research Cluster
Zip code
Address
4-9-1 Anagawa, Inage-ku, Chiba, Chiba 263-8555, Japan
TEL
043-206-3025
Homepage URL
suzuki.kazuko@qst.go.jp
Sponsor or person
Institute
National Institute of Radiological Sciences
Institute
Department
Personal name
Funding Source
Organization
National Institute of Radiological Sciences
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
| 2016 | Year | 06 | Month | 30 | 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
Terminated
Date of protocol fixation
| 2016 | Year | 06 | Month | 27 | Day |
Date of IRB
Anticipated trial start date
| 2016 | 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
| 2016 | Year | 06 | Month | 29 | Day |
Last modified on
| 2018 | Year | 07 | Month | 02 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000026422
