Post-marketing Surveillance of Long-term Administration of Donepezil Hydrochloride -Investigation of the Clinical Condition and Safety in Patients With Alzheimer's Disease-

Eisai Co., Ltd.10,238 enrolled

Overview

The purpose of this study is to investigate the following about donepezil hydrochloride administration in patients with mild or moderate Alzheimer's Disease in clinical practice: cognitive function, Functional Assessment Staging (FAST) score, adverse events/adverse drug reactions, and patient background.

Study Type

OBSERVATIONAL

Enrollment

10,238

Conditions

Alzheimer's Disease

Interventions

donepezil hydrochlorideDRUG

This is a multicenter, open-labeled, practice-based, post-marketing surveillance study. Therefore, dosing is not specified.

Eligibility

Sex: ALL

Medical Language ↔ Plain English

Inclusion criteria: Patients diagnosed with Alzheimer's Disease by Diagnostic and Statistical Manual of Mental Disorders (DSM-IV). Patients diagnosed with mild or moderate Alzheimer's Disease, applicable to FAST score 4 or 5. Exclusion criteria: Patients with history of hypersensitivity to component of Aricept or piperidine derivative. Patients registered for this survey before.

Locations (722)

Outcomes

Primary Outcomes

The transition of clinical condition is evaluated comparing the result of HDS-R,MMSE with the time of study initiation

Time frame: 48 months(12 weeks and every 6 months)

Data from ClinicalTrials.gov

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Unnamed facility

Aisai, Aichi-ken, Japan

Unnamed facility

Chita, Aichi-ken, Japan

Unnamed facility

Gamagōri, Aichi-ken, Japan

Unnamed facility

Handa, Aichi-ken, Japan

Unnamed facility

Ichinomiya, Aichi-ken, Japan

Unnamed facility

Inazawa, Aichi-ken, Japan

Unnamed facility

Inuyama, Aichi-ken, Japan

Unnamed facility

Kariya, Aichi-ken, Japan

Unnamed facility

Kasugai, Aichi-ken, Japan

Unnamed facility

Komaki, Aichi-ken, Japan

...and 712 more locations