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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02267486
Other study ID # TRIAD1402
Secondary ID UMIN000016394
Status Completed
Phase N/A
First received October 14, 2014
Last updated July 14, 2016
Start date October 2014

Study information

Verified date July 2016
Source Translational Research Informatics Center, Kobe, Hyogo, Japan
Contact n/a
Is FDA regulated No
Health authority Japan: Central ethics board
Study type Observational

Clinical Trial Summary

Examine the construct validity, the group discriminant ability, and the inter-rater reliability of a novel dementia rating scale (QuQu scale: QUick QUestion scale) candidate for the evaluation of patients with Alzheimer Dementia (AD)


Recruitment information / eligibility

Status Completed
Enrollment 972
Est. completion date
Est. primary completion date March 2016
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

1. Alzheimer Dementia (AD) patients and patients with cognitive concern without dementia

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:

1. patients with other types of dementia (e.g. vascular dementia, Levy body dementia, frontotemporal dementia)

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)

Study Design

Time Perspective: Prospective


Related Conditions & MeSH terms


Intervention

Other:
Standard therapy of Alzheimer Dementia (AD)

Observation


Locations

Country Name City State
Japan Kagawa University School of Medicine Kida-gun Kagawa

Sponsors (2)

Lead Sponsor Collaborator
Translational Research Informatics Center, Kobe, Hyogo, Japan Daiichi Sankyo Co., Ltd.

Country where clinical trial is conducted

Japan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Novel Dementia Rating Scale (QUick QUestion Scale) 1 day No
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