drugset / Trial / NCT00576732

A Study of the Effectiveness and Safety of Two Doses of Risperidone in the Treatment of Children and Adolescents With Autistic Disorder

NCT00576732

RandomizedParallel-groupTriple-blindTreatment

Summary

The purpose of this study is to evaluate the effectiveness (change in level of irritability and related behaviors) and safety and tolerability of the administration of 2 different fixed dose levels of risperidone (an atypical antipsychotic drug) compared with placebo in children or adolescents who have autism, and to evaluate the safety and tolerability of the drug for additional 26 weeks after the initial 6-week study period.

Timeline

Start
2007-12
Primary completion
2009-09
Completion
2010-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Risperidone Other / unclassified 0.125 mg Oral
Subject Risperidone Other / unclassified 0.175 mg Oral
Subject Risperidone Other / unclassified 1.25 mg Oral
Subject Risperidone Other / unclassified 1.75 mg Oral

Indications