drugset / Trial / NCT00088075

Investigate Risperidone for the Treatment of Schizophrenia in Adolescents

NCT00088075

RandomizedParallel-groupDouble-blindTreatment

Summary

A clinical study to evaluate the efficacy, safety and tolerability of two dose ranges of risperidone (1 to 3 mg/day, and 4 to 6 mg/day) versus placebo (an inactive substance like a sugar pill) in adolescents (aged 13 to 17 years) with schizophrenia (i.e. abnormal behavior and thoughts). The study duration is about 6 to 7 weeks.

Timeline

Start
2004-08
Primary completion
Completion
2005-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Risperidone Other / unclassified 1 mg Oral
Subject Risperidone Other / unclassified 3 mg Oral
Subject Risperidone Other / unclassified 4 mg Oral
Subject Risperidone Other / unclassified 6 mg Oral

Indications