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Autism and Communication


Clinical Trial: Drug Treatment for Autism

This study is currently recruiting patients.

Sponsored by: National Institute of Mental Health (NIMH)
Information provided by: National Institute of Mental Health (NIMH)

Purpose

The purpose of this study is to examine the safety and effectiveness of donepezil HCl (Aricept) in children and adolescents with Autism Spectrum Disorder (ASD).

Condition Treatment or Intervention Phase
Autistic Disorder
 Drug: Donepezil HCl
Phase I

MedlinePlus related topics:  Autism

Study Type: Interventional
Study Design: Treatment, Randomized, Double-Blind, Placebo Control, Parallel Assignment, Safety/Efficacy Study

Official Title: Donepezil HCl: Treating Cognitive Deficits in Autism

Further Study Details: 

Expected Total Enrollment:  40

Study start: October 2002;  Expected completion: August 2005

Children with autism spectrum disorder (ASD) often have impaired communication, problems with social interaction, and repetitive and stereotyped patterns of behavior. While most research has attempted to treat the behavioral deficits commonly associated with ASD, few studies have attempted to improve the core features of this disorder. A recent study found that donepezil HCl helped to improve speech production, attention span, and ability to express emotions in a group of children with autism. This study will provide an opportunity to conduct further testing of the effects of donepezil HCl on the cognitive deficits presumed to underlie the core features of ASD.

This study begins at Week 1 with a baseline assessment. Participants are then randomly assigned to either donepezil HCl or placebo. Participants will start with either a 5mg/day dose of donezepil HCl or placebo followed by a cognitive assessment after 4 weeks on this dose. Participants will then have their dose increased to 10mg/day. Another cognitive assessment will be given after 4 weeks on this dose.

Eligibility

Ages Eligible for Study:  8 Years   -   17 Years,  Genders Eligible for Study:  Both

Criteria

Inclusion Criteria:

  • Autism Spectrum Disorder (ASD)
  • Asperger's Disorder
  • IQ of 75 or above
  • Baseline assessment tests within the acceptable range

Exclusion Criteria:

  • Bipolar disorder, schizophrenia, schizoaffective disorder, or psychotic disorder
  • Seizure disorder requiring the use of anticonvulsant medications
  • Congenital rubella, cytomegalovirus, or tuberous sclerosis
  • Certain medications prescribed for management of behavior (please contact the investigator for a complete list)
  • Medications/preparations that are known to interact with donepezil HCl
  • Significant medical illness, endocrinopathies, cardiovascular disease, or severe chronic malnutrition
  • Pregnancy or sexually active females not using a reliable method of contraception

Location and Contact Information

Benjamin L Handen, PhD      412-235-5445    handenbl@msx.upmc.edu
Sarah McAuliffe-Bellin, M.Ed.      412-235-5447    mcauliffebellnsj@msx.upmc.edu

Pennsylvania
      Western Psychiatric Institute & Clinic, Pittsburgh,  Pennsylvania,  15213,  United States; Recruiting
Benjamin L Handen, Ph.D.  412-235-5445    handenbl@msx.upmc.edu 
Sarah McAuliffe-Bellin, M.Ed.  412-235-5447    mcauliffebellinsj@msx.upmc.edu 
Benjamin L Handen, Ph.D.,  Principal Investigator
Antonio Y Hardan, M.D.,  Sub-Investigator
Cynthia R Johnson, Ph.D.,  Sub-Investigator

Study chairs or principal investigators

Benjamin L. Handen, Ph.D.,  Principal Investigator,  University of Pittsburgh, School of Medicine, Department of Psychiatry   

More Information

Study ID Numbers:  NIMH-65941-01
Record last reviewed:  December 2004
Last Updated:  December 6, 2004
Record first received:  October 11, 2002
ClinicalTrials.gov Identifier:  NCT00047697
Health Authority: United States: Federal Government
ClinicalTrials.gov processed this record on 2005-04-08


Source: ClinicalTrials.gov
Cache Date: April 9, 2005


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Page Updated: September 6, 2005
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