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Completed Phase 3 Interventional

Efficacy and Safety of Aricept in the Treatment of Severe Alzheimer's Disease

ClinicalTrials.gov ID: NCT00096473

Public ClinicalTrials.gov record NCT00096473. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 22, 2026, 9:51 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A 24 Week, Multicenter, Randomized, Double-Blind, Placebo-Controlled Evaluation of the Safety and Efficacy of Donepezil Hydrochloride (E2020) in Patients With Severe Alzheimer's Disease Followed by a 12 Week Open-Label Extension Period

Study identification

NCT ID
NCT00096473
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Eisai Inc.
Industry
Enrollment
229 participants

Conditions and interventions

Interventions

  • Donepezil hydrochloride Drug

Drug

Eligibility (public fields only)

Age range
50 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Dec 31, 2000
Primary completion
May 31, 2005
Completion
Aug 31, 2005
Last update posted
Mar 31, 2011

2001 – 2005

United States locations

U.S. sites
28
U.S. states
17
U.S. cities
28
Facility City State ZIP Site status
Not listed Northport Alabama
Not listed Phoenix Arizona
Not listed Sun City Arizona
Not listed Tucson Arizona
Not listed San Francisco California
Not listed Santa Monica California
Not listed Torrance California
Not listed Denver Colorado
Not listed Fort Lauderdale Florida
Not listed Fort Myers Florida
Not listed North Miami Florida
Not listed St. Petersburg Florida
Not listed Atlanta Georgia
Not listed Chicago Illinois
Not listed New Orleans Louisiana
Not listed Springfield Massachusetts
Not listed Long Branch New Jersey
Not listed Piscataway New Jersey
Not listed New Hyde Park New York
Not listed Greenville North Carolina
Not listed Raleigh North Carolina
Not listed Centerville Ohio
Not listed Oklahoma City Oklahoma
Not listed Medford Oregon
Not listed Portland Oregon
Not listed Jenkintown Pennsylvania
Not listed Austin Texas
Not listed Houston Texas

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 14 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00096473, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Mar 31, 2011 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00096473 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →