N/A
N=13
Efficacy of Aripiprazole Versus Placebo in the Reduction of Aggressive and Aberrant Behavior in Autistic Children
Autism
Bottom Line
View on ClinicalTrials.gov: NCT00468130 ↗Enrolled (actual)
13
Serious AEs
0.0%
Results posted
Jan 2022
Primary outcome: Primary: Clinical Global Impression Improvement (CGI-AD) — 3.83; 4.25; 2.67; 4.25 score on a scale
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Aripiprazole (Drug); Placebos (Drug)
- Age
- Pediatric · 5+ yrs
- Sex
- All
- Sponsor
- University of Medicine and Dentistry of New Jersey
- Primary completion
- Nov 2009
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Clinical Global Impression Improvement (CGI-AD) |
3.83; 4.25; 2.67; 4.25 | — |
| SECONDARY Aberrant Behavior Checklist |
15.67; 8.00; 6.83; 8.67 | — |
Summary
Hypothesis: (1) Aripiprazole treatment will be superior to placebo in reducing aggression and irritability in autistic individuals as shown by reductions in the Aberrant Behavior Checklist-irritability subscale.
(2) Aripiprazole treatment will be superior to placebo in the acute treatment of global autism severity.
The purpose of this study is to examine the possible benefit of the medication Aripiprazole in autistic individuals.
Eligibility Criteria
Inclusion Criteria
- Meets DSM-IV, ADI-R criteria for autistic disorder.
- Age 5-17 years.
- Outpatients
- Parent or legal guardian willing to sign informed consent.
Exclusion Criteria
- Subject has been diagnosed with a psychotic disorder (such as schizophrenia) or a mood disorder, including depression or bipolar disorder (manic depression).
- Subject has caused visible harm to him/herself.
- Subject has an active seizure disorder or epilepsy (seizures within the past year).
- Subject has an unstable medical illness, including heart disease.
- Subject has experienced brain injury.
- Subject has a history of diabetes.
- Subject reports significant improvement of autism symptoms and behaviors to current medication or other therapies.
- Subject has a history of prior treatment with Aripiprazole of 5 mg/day or higher for 6 weeks.
- Subject lives in a far away area and/or does not have regular access to transportation to the clinical facility.
- Subject is a pregnant female or unwilling to use acceptable contraception if sexually active.
Data sourced from ClinicalTrials.gov (NCT00468130). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.