Multiple Locations, Japan
NCT Number: NCT02162264
Post-marketing Surveillance of Donepezil Hydrochloride -Investigation of the Factors That Affect Aricept Medication Persistence Rate and the Safety and Efficacy in Patients With Alzheimer's Disease in Clinical Practice
To investigate the factors that affect Aricept medication persistence rate and the safety and efficacy in patients with Alzheimer's Disease in clinical practice
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Notify MeKey information
Conditions
Sex eligibility
All sexes
Study type
Observational
Primary location
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Patients diagnosed with Alzheimer's Disease and administered Aricept for the first time.
Exclusion criteria
Patients with a history of hypersensitivity to any ingredients of Aricept or piperidine derivatives.
Treatment and study plan
Donepezil Hydrochloride
DrugInitial dose of 3 mg orally once daily. After 1-2 weeks, dosage increased to 5 mg orally once daily. After 4 or more weeks, dosage increased to 10 mg orally once daily for patients with severe dementia of Alzheimer's type. Dose reduced appropriately according to patient's symptoms.
Other names: Aricept
Primary outcomes
-
Change From Baseline in the Mini-Mental State Examination (MMSE) Score
Time frame: Baseline, Month 3, Month 6, and Month 12
Secondary outcomes
-
Investigations on adverse events and adverse drug reactions
Time frame: Baseline and Month 12
Sponsors and collaborators
Lead sponsor
Eisai Co., Ltd.
Industry
Registry information
Important dates
- Study start
- 2013
- Primary completion
- 2015
- Study completion
- 2016
- First posted
- Jun 12, 2014
- Registry last updated
- Sep 7, 2018
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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