Randomized, Double-Blind, Placebo-Controlled Study of Efficacy and Safety of Donepezil Hydrochloride in Preadolescent and Adolescent Children With Attention Impairment Following Cancer Treatment

The purpose of this study is to evaluate the efficacy, safety and tolerability of donepezil in children with persistent attention impairment that is present at least 12 months after the completion of cancer treatment.

Stanford is not currently accepting new patients for this trial. You may want to check clinicaltrials.gov to see if other locations are recruiting.

Investigator(s):

Intervention(s):

  • drug : Placebo
  • drug : Donepezil hydrochloride

Phase: Phase 3

Eligibility

Ages Eligible For Study:

6 Years - 17 Years

External Links

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Contact information

Primary Contact:

Jennifer Lew 6507254318

Stanford University School of Medicine 300 Pasteur Drive Stanford, CA 94305

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