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CompletedPhase 4

Efficacy and Safety of Donepezil Hydrochloride (Aricept) in Vascular Dementia

An Open Label Study on the Efficacy and Safety of Donepezil Hydrochloride (Aricept) in Vascular Dementia

Lead sponsor

Eisai Inc.

Asset

Donepezil

Listed sites

2

Recruiting sites

-

Enrollment

36

actual

Study population

Vascular cognitive impairment / dementia

Key I/E criteria

Vascular dementiaStudy partner/caregiver required

Primary endpoint

Clinician's Interview Based Impression of Change-Plus Caregiver Input

Footprint

Where this trial recruits

Site locations as reported to ClinicalTrials.gov. Site count is not enrollment count; per-site enrollment is not available from source.

Identifiers

Registered as

Org study IDAS-005 (ART-MNL-05-02)
NCT IDNCT00165763

Timeline

Milestones

Study start2005-09 (month precision)
Study first posted2005-09-14estimated
Primary completion2009-09actual (month precision)
Last update posted2012-05-04estimated

Assets

Drug assets

Study populations

Who this study enrolls

Vascular cognitive impairment / dementia

Eligibility

Who can enroll

Minimum age40 Years
Maximum age60 Years
SexAll
Healthy volunteersNot accepted

Inclusion criteria

The subjects eligible for this study are men and women outpatients, age 40-60 years old, who fulfill the criteria for VAD according to the National Institute of Neurological Disorders and Stroke and the Association Internationale pour la Recherche et l'Enseignement en Neurosciences International Workshop (NINCDS-AIREN). Subjects shall undergo extensive clinical examination by a stroke specialist and radiological examination (CT or MRI) to document presence of cerebrovascular disease. The clinical diagnosis has to be relevant to the imaging findings.

Other Inclusion criteria:

Subjects with clinically stable hypertension, diabetes mellitus, and cardiac disease for the last 3 months. Subjects with history of recent stroke, who have not been hospitalized for stroke in the previous 3 months. Subjects with depression controlled with medications. Subjects should have no hearing or visual impairment and live with a reliable caregiver

Exclusion criteria

Subjects should have no radiological evidence of other brain disorders (subdural hematoma, post-traumatic / post-surgery) have no depression or other psychiatric disorders, infectious disorders, neoplastic condition, and metabolic and toxic encephalopathies, dementia due to AD or prior diagnosis of AD, and major depression or other psychiatric disorders.

Subjects with clinical evidence of pulmonary, hepatic, gastrointestinal, metabolic, endocrine or other life threatening diseases; pregnancy, history of alcohol or drug abuse, and sensitivity to cholinesterase inhibitors; use of investigational agents, cholinomimetic and anticholinergic agents.

Endpoints (2)

What's being measured

Protocol endpoints and posted registry outcome measures, grouped into outcome categories. Composite endpoints show their component event types. Standard codes (LOINC, SNOMED CT) are shown where available.

Coverage by outcome category

Caregiver / quality of life
1
Other (unclassified)
1

Caregiver / quality of life

1 endpoint
Primary/protocol endpoint

Clinician's Interview Based Impression of Change-Plus Caregiver Input (CIBIC-Plus).

Time frame:6,12,18, 24 weeks.

descriptive

Other (unclassified)

1 endpoint
Secondary/protocol endpoint/low confidence

Vascular Dementia Assessment Scale cognitive subscale (VaDAS-cog).

Time frame:6,12,18, 24 weeks.

ADAS-Cog

descriptive

Provenance

Sources

Trial identity, design, statusClinicalTrials.gov API v2
Snapshot dateJuly 21, 2026
Endpoint classificationDelfa ADRD endpoint taxonomy
Results tableno registry results posted yet

Trial facts come from public ClinicalTrials.gov records. Endpoint categories are Delfa's classification of those records, not a ClinicalTrials.gov field. All figures reflect the July 21, 2026 snapshot.