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CompletedPhase 4

Electrophysiologic Measures of Treatment Response in Alzheimer Disease

Verbal Memory ERPs as Indices of Treatment Response in Alzheimer Disease

Assets

Donepezil / Nicotine / Rivastigmine

Listed sites

1

Recruiting sites

-

Enrollment

-

Study population

Alzheimer’s disease

Key I/E criterion

Alzheimer's disease

Primary endpoint

-

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 IDAGCG-004-98S
NCT IDNCT00018278

Timeline

Milestones

Study start1998-10 (month precision)
Study first posted2001-07-05estimated
Study completion2001-09 (month precision)
Last update posted2009-01-21estimated

Assets

Drug assets

Study populations

Who this study enrolls

Alzheimer’s disease

Eligibility

Who can enroll

Minimum age55 Years
Maximum age85 Years
SexAll
Healthy volunteersAccepted

Eligibility criteria

Patients diagnosed with mild to moderate probable Alzheimer's disease (mini-mental state exam scores between 15-27), and normal controls (age generally between 60-85). Subjects must either be planning to start daily cholinesterase therapy (e.g. Aricept, Exelon) or willing to try a transdermal nicotine patch for two 8 hour periods.

Endpoints (0)

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.

No endpoints recorded for this trial.

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.