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Trials / Completed

CompletedNCT00293176

The Evaluation of the Efficacy and Safety of Donepezil Hydrochloride in Subjects With Mild Cognitive Impairment (MCI)

A One-Year, Multicenter, Randomized, Double-Blind, Placebo-Controlled Evaluation of the Efficacy and Safety of Donepezil Hydrochloride in Subjects With Mild Cognitive Impairment (MCI)

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
821 (actual)
Sponsor
Eisai Inc. · Industry
Sex
All
Age
45 Years – 90 Years
Healthy volunteers
Not accepted

Summary

To investigate the efficacy and safety of donepezil in individuals with mild cognitive impairment on measures of cognition, global function and behavior.

Conditions

Interventions

TypeNameDescription
DRUGDonepezil HydrochlorideSubects will receive a starting dose of 5 mg orally. Dose-escalation from 5 mg to 10 mg will occur at the Week 9 Visit.
DRUGPlaceboSubjects will receive matching placebo tablets.

Timeline

Start date
2003-12-01
Primary completion
2007-03-01
Completion
2007-03-01
First posted
2006-02-17
Last updated
2011-04-01

Locations

54 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT00293176. Inclusion in this directory is not an endorsement.

The Evaluation of the Efficacy and Safety of Donepezil Hydrochloride in Subjects With Mild Cognitive Impairment (MCI) (NCT00293176) · Clinical Trials Directory