Open Label Trial of Aripiprazole in Children and Adolescents With Tourette's Disorder

Last updated: October 26, 2016
Sponsor: NYU Langone Health
Overall Status: Completed

Phase

4

Condition

Tourette's Syndrome

Autism

Tic Disorders

Treatment

N/A

Clinical Study ID

NCT00241176
H12189
  • Ages 7-18
  • All Genders

Study Summary

The purpose of this study is to determine if Abilify will reduce tics (repetitive, uncontrollable movements or vocalizations) in children and adolescents ages 7-18 with Tourette's Disorder (TD) or a chronic motor tic disorder (either repetitive, uncontrollable movements or vocalizations).

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Child or adolescent must be 7 to 18 years of age (inclusive) when informed consent isobtained.

  • Must meet full criteria for Tourette's Disorder or chronic motor tic disorder.

  • Must have failed to respond to an adequate trial, as determined by the investigator,of clonidine, guanfacine, or neuroleptic medication in the past.

  • Tics are causing significant distress or impairment, as determined by parent/subjectand principal investigator, on current treatment regimen.

  • Laboratory results, including serum chemistries, hematology, and urinalysis, must showno significant abnormalities (significant is defined as laboratory values requiringacute medical intervention).

  • Must be able to swallow pills.

  • Must be of normal intelligence in the judgment of the investigator.

  • Must possess an educational level, degree of understanding and command of the Englishlanguage to enable them to communicate suitably with the investigator and studycoordinator, and to understand the nature of the study.

  • Subjects and their legal representatives must be considered reliable.

  • Written informed consent of parents and subjects (ages 18 and above) and assent ofsubjects ages 7-17 will be obtained.

Exclusion

Exclusion Criteria:

  • Organic brain disease, for example, traumatic brain injury residua.

  • Mental retardation as defined by the DSM-IV-TR.

  • A history of seizure disorder (other than febrile seizure).

  • A history of Sydenham's Chorea.

  • Autism, schizophrenia, other psychotic disorder, or bipolar disorder.

  • A primary diagnosis of a major mood disorder that requires ongoing psychiatrictreatment.

  • A neurological disorder other than a tic disorder.

  • A major medical illness.

  • Females who are of child bearing age who are unwilling to use birth control or who arepregnant, as determined by serum pregnancy test at baseline assessment, or lactating.

  • Have a past or current history of substance dependence and/or a current history ofsubstance abuse or who fail baseline toxic screen.

  • Have any clinically significant abnormal laboratory result at baseline screeningincluding EKG, or blood tests.

  • Have a history of ongoing or previously undisclosed child abuse (risk of removal fromhome would not allow for consistent caretaker ratings).

Study Design

Total Participants: 11
Study Start date:
September 01, 2005
Estimated Completion Date:
February 28, 2010

Study Description

The aims of this study are to obtain systematic data regarding dosing and safety of aripiprazole (Abilify) in the treatment of youth with Tourette's Disorder (TD). Tourette's Disorder is characterized by multiple motor (more than one uncontrollable movement) and vocal tics (vocal outbursts) which have been present for more than 1 year, with onset before the age of 18. The disorder causes marked distress in social, occupational or other important areas of functioning. Abilify has been approved by the United States Food and Drug Administration (FDA) to treat adults with schizophrenia but has not been approved to treat Tourette's Disorder (TD) so it is considered experimental or investigational in this study.

Connect with a study center

  • NYU Child Study Center

    New York, New York 10016
    United States

    Site Not Available

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