The purpose of this study is to examine the efficacy and safety of cholinesterase inhibitor (donepezil hydrochloride) Aricept in patients with vascular dementia (VaD).
Vascular dementia is a significant cause of intellectual and functional impairment in young patients consequent to cerebrovascular disease. Post-mortem studies show that VaD patients have a cholinergic deficiency like in Alzheimer's disease (AD). Cholinesterase inhibitors are now standard treatment for mild to moderate AD. This study aims to determine if donepezil, a cholinesterase inhibitor, would benefit patients with VaD by decreasing their scores in the VaDAS-cog and improvement in their CIBIC rating over a period of 24-weeks treatment. Adverse events will also be monitored.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
36
5 mg donepezil HCl given once a day and increased to 10 mg per day if side effects, when present, are tolerated.
Memory Center
Quezon, Manila, Philippines
Subic Bay Medical Center
Olongapo City, Zambales, Philippines
Clinician's Interview Based Impression of Change-Plus Caregiver Input (CIBIC-Plus).
Time frame: 6,12,18, 24 weeks.
Vascular Dementia Assessment Scale cognitive subscale (VaDAS-cog).
Time frame: 6,12,18, 24 weeks.
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