drugset / Trial / NCT00378092

A Follow-Up Study of Schizophrenic Participants Following Treatment Discontinuation After Remission From a First Psychotic Episode

NCT00378092

Phase 4 Completed 33 enrolled Janssen Cilag N.V./S.A.
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the outcome of medication discontinuation, the safety and effectiveness of re-initiating risperidone long acting injection (RLAI) in case of relapse (the return of a medical problem) of schizophrenia (psychiatric disorder with symptoms of emotional instability, detachment from reality, often with delusions and hallucinations, and withdrawal into the self) during the study observation period of 36 months.

Timeline

Start
2006-04
Primary completion
2010-03
Completion
2010-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Risperidone Other / unclassified 1 mg Oral
Subject Risperidone Other / unclassified 2 mg Oral
Subject Risperidone Other / unclassified 3 mg Oral
Subject Risperidone Other / unclassified 25 mg Oral
Subject Risperidone Other / unclassified 37.5 mg Oral
Subject Risperidone Other / unclassified 50 mg Oral

Indications