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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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JPRN |
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Last refreshed on:
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17 October 2023 |
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Main ID: |
JPRN-UMIN000014098 |
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Date of registration:
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01/06/2014 |
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Prospective Registration:
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Yes |
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Primary sponsor: |
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Public title:
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Clinical study for degenerative dementia
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Scientific title:
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Clinical study for degenerative dementia - Degenerative dementia clinical study |
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Date of first enrolment:
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2014/06/01 |
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Target sample size:
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150 |
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Recruitment status: |
Complete: follow-up complete |
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URL:
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https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000016388 |
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Study type:
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Interventional |
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Study design:
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Single arm Non-randomized
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Phase:
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Not applicable
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Countries of recruitment
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Japan
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Contacts
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Name:
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Yumiko Motoi |
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Address:
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Bunkyo-ku Hongo 2-3-18 Regalo Ochanomizu II 602
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Telephone:
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+81-3-5689-8556 |
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Email:
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motoi@juntendo.ac.jp |
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Affiliation:
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Juntendo University school of Medicine Department of Diagnosis, Prevention and Treatment of Dementia |
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Name:
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Yumiko Motoi |
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Address:
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Bunkyo-ku Hongo 2-3-18 Regalo Ochanomizu II 602
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Telephone:
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+81-3-5689-8556 |
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Email:
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motoi@juntendo.ac.jp |
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Affiliation:
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Juntendo University school of Medicine Department of Diagnosis, Prevention and Treatment of Dementia |
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Key inclusion & exclusion criteria
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Inclusion criteria:
Exclusion criteria: 1) Cognitive dysfunction, systemic diseases or central nervous system other than CBS, PPA, and DLB (Schizophrenia, Bipolar disorder, Parkinson's disease, Vascular dementia, Huntington disease, brain tumor, Pick disease, Creutzfeldt-Jakob disease,Normal pressure hydrocephalus, Progressive supranuclear palsy,cerebral stroke, subdural hematoma, multiple sclerosis, epilepsy, HIV infection, neurosyphilis) 2. In the presence of any other physical illness such as Vitamine deficiency 3. In case physicians judge that the participants are mismatched.
Age minimum:
40years-old
Age maximum:
90years-old
Gender:
Male and Female
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Health Condition(s) or Problem(s) studied
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Corticobasal syndrome, Primary progressive aphasia, Dementia with Lewy bodies
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Intervention(s)
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Neuropshychological tests and Dopamine transporter scan
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Primary Outcome(s)
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Dopamine transporter scan
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Secondary Outcome(s)
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Neurospychological battery
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Source(s) of Monetary Support
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Grants-in-Aid for Scientific Research
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Ethics review
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Status: YES
Approval date:
Contact:
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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