Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
972 participants
OBSERVATIONAL
2014-10-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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PROSPECTIVE
Study Groups
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Alzheimer Dementia (AD)
Patients with dementia caused by Alzheimer's disease
Standard therapy of Alzheimer Dementia (AD)
Non-dementia
Patients with cognitive concern without dementia
Observation
Interventions
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Standard therapy of Alzheimer Dementia (AD)
Observation
Eligibility Criteria
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Inclusion Criteria
2. Written Informed consent by each subject and/or a legal representative, and study informant. If the doctor decides that the patient has no trouble in understanding this study, the written informed consent of a legal representative may be exempted. If not, this study needs a written informed consent by a legal representative and the patient except the case where the consent is hardly obtained due to the progression of the disease.
Exclusion Criteria
2. patients with other diseases which cause secondary dementia prior to Alzheimer Dementia (AD)
3. patients with other severe neurological disease or psychiatric disorder without Alzheimer Dementia (AD)
4. patients with other medical conditions where the investigators determine that it is inappropriate for the subject of this study (e.g. inappropriate for the evaluation of dementia rating scale)
ALL
No
Sponsors
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Daiichi Sankyo Co., Ltd.
INDUSTRY
Translational Research Center for Medical Innovation, Kobe, Hyogo, Japan
OTHER
Responsible Party
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Principal Investigators
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Yu Nakamura
Role: PRINCIPAL_INVESTIGATOR
Kagawa University School of Medicine
Locations
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Kagawa University School of Medicine
Kida-gun, Kagawa-ken, Japan
Countries
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Other Identifiers
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UMIN000016394
Identifier Type: OTHER
Identifier Source: secondary_id
TRIAD1402
Identifier Type: -
Identifier Source: org_study_id
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