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Phase 3 Randomized Placebo Controlled Clinical Trial of Donepezil

This study is to compare the safety and effects of donepezil (Aricept) for patients reporting cognitive or memory issues after receiving chemotherapy for breast cancer. Patients will receive either donepezil or placebo for 24 weeks. The primary objective is to see if memory improves with the use of donepezil during the study.

Research Base: Wake Forest University Health Sciences
NCT ID: NCT02822573
NCI Protocol Number: WF-97116
Status: Recruiting

For more information see



Cognitive Dysfunction, Memory Impairment

Trial Type

Supportive Care/Symptom Management/PROs

See a list of participating sites on