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CompletedPhase 3

Safety of Donepezil in Patients With Dementia Associated With Cerebrovascular Disease

Open-Label, Multicentre, One Year Extension of the Evaluation of the Safety of Donepezil Hcl in Patients With Dementia Associated With Cerebrovascular Disease

Asset

Donepezil

Listed sites

1

Recruiting sites

-

Enrollment

-

Study population

Vascular cognitive impairment / dementia

Key I/E criterion

•Age ≥45

Primary endpoint

•Safety assessments

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 ID03-0725-AE
SecondaryE2020-A001-320
NCT IDNCT00188812

Timeline

Milestones

Study start2004-05 (month precision)
Study completion2005-08 (month precision)
Study first posted2005-09-16estimated
Last update posted2009-01-12estimated

Assets

Drug assets

Donepezil

Study populations

Who this study enrolls

Vascular cognitive impairment / dementia

Eligibility

Who can enroll

Minimum age45 Years
SexAll

Inclusion criteria

•must have completed previous study E2020-A001-319

Exclusion criteria

•absence of a reliable caregiver
•clinically significant medical condition
•recent TIA

Endpoints (1)

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.

Safety / tolerability / PK

1 endpoint
Primary/protocol endpoint

safety assessments

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.