UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000042119 |
|---|---|
| Receipt number | R000048070 |
| Scientific Title | Reproducibility of a novel method of measuring brain volume using MRI (MRI-TAISEKI) |
| Date of disclosure of the study information | 2020/10/15 |
| Last modified on | 2020/10/14 15:56:50 |
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Basic information
Public title
Reproducibility of a novel method of measuring brain volume using MRI (MRI-TAISEKI)
Acronym
Study on reproducibility of MRI-TAISEKI analysis
Scientific Title
Reproducibility of a novel method of measuring brain volume using MRI (MRI-TAISEKI)
Scientific Title:Acronym
Study on reproducibility of MRI-TAISEKI analysis
Region
| Japan |
Condition
Condition
Healthy volunteer
Classification by specialty
| Psychiatry |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
The purpose of this study is to evaluate the reproducibility of MRI-TAISEKI, a new brain volume measurement method being developed by NIHON TECTSYSTEMS, in healthy subjects.
Basic objectives2
Others
Basic objectives -Others
N/A
Trial characteristics_1
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
The intraclass correlation coefficient (ICC) of the hippocampal volume obtained by "MRI-TAISEKI".
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
| 20 | years-old | <= |
Age-upper limit
| 75 | years-old | > |
Gender
Male and Female
Key inclusion criteria
1) Male or female
2) Those between the ages of 20 and 75
3) No psychiatric or neurological disorders based on the doctor's interview
4) No contraindications to MRI scans
Key exclusion criteria
1) Patients with a history of psychiatric disorders as defined in DSM 5.
2) Patients with a history of cerebral tumor, cerebral hemorrhage, or cerebral infarction.
3) Patients with severe physical illness.
Target sample size
15
Research contact person
Name of lead principal investigator
| 1st name | Fumitoshi |
| Middle name | |
| Last name | Kodaka |
Organization
The Jikei University School of Medicine
Division name
Department of Psychiatry
Zip code
105-8471
Address
3-25-8 Nishi-shinbashi, Minato-ku, Tokyo 105-8471, Japan
TEL
03-3433-1111
kodaka@jikei.ac.jp
Public contact
Name of contact person
| 1st name | Fumitoshi |
| Middle name | |
| Last name | Kodaka |
Organization
The Jikei University School of Medicine
Division name
Department of Psychiatry
Zip code
105-8471
Address
3-25-8 Nishi-shinbashi, Minato-ku, Tokyo 105-8471, Japan
TEL
03-3433-1111
Homepage URL
kodaka@jikei.ac.jp
Sponsor or person
Institute
The Jikei University School of Medicine
Institute
Department
Personal name
Funding Source
Organization
The Jikei University School of Medicine
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
The Jikei University School of Medicine
Address
3-25-8 Nishi-shinbashi, Minato-ku, Tokyo 105-8471, Japan
Tel
03-3433-1111
kodaka@jikei.ac.jp
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
| 2020 | Year | 10 | 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
15
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
No longer recruiting
Date of protocol fixation
| 2020 | Year | 02 | Month | 06 | Day |
Date of IRB
| 2020 | Year | 02 | Month | 06 | Day |
Anticipated trial start date
| 2020 | Year | 06 | Month | 01 | Day |
Last follow-up date
| 2021 | Year | 04 | Month | 30 | Day |
Date of closure to data entry
Date trial data considered complete
Date analysis concluded
Other
Other related information
N/A
Management information
Registered date
| 2020 | Year | 10 | Month | 14 | Day |
Last modified on
| 2020 | Year | 10 | Month | 14 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000048070
| Research Plan | |
|---|---|
| Registered date | File name |
| Research case data specifications | |
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| Registered date | File name |
| Research case data | |
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| Registered date | File name |
