drugset / Trial / NCT00249132

A Study of the Effectiveness and Safety of Risperidone Compared With Haloperidol and Placebo in Patients With Chronic Schizophrenia

NCT00249132

Phase 3 Completed 523 enrolled Janssen, LP
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of the study is to evaluate the effectiveness and safety of different doses of risperidone (an antipsychotic medication) compared with placebo and with a fixed 20 mg/day dose of a standard antipsychotic, haloperidol, in patients with chronic schizophrenia.

Timeline

Start
Primary completion
Completion
1991-07

Drugs

EvaluationDrugModalityDoseRoute
Subject Risperidone Other / unclassified 2 mg Oral
Subject Risperidone Other / unclassified 6 mg Oral
Subject Risperidone Other / unclassified 10 mg Oral
Subject Risperidone Other / unclassified 16 mg Oral

Indications