Overview

Oral Versus Injectable Risperidone for Treating First-Episode Schizophrenia

Status:
Completed
Trial end date:
2012-11-01
Target enrollment:
0
Participant gender:
All
Summary
This study will determine the effectiveness of oral risperidone versus long-acting injectable risperidone in treating people with first-episode schizophrenia.
Phase:
Phase 4
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
University of California, Los Angeles
Collaborators:
Janssen Scientific Affairs, LLC
National Institute of Mental Health (NIMH)
Ortho-McNeil Janssen Scientific Affairs, LLC
Treatments:
Risperidone
Criteria
Inclusion Criteria:

- DSM-IV diagnosis of schizophrenia, schizoaffective disorder (depressed type), or
schizophreniform disorder

- First major episode of psychotic symptoms occurred within 2 years prior to study entry

- Participant in the UCLA Center for Neurocognition and Emotion in Schizophrenia

Exclusion Criteria:

- Neurological disorder or injury (e.g., encephalitis, epilepsy, traumatic brain injury)

- Mental retardation (e.g., premorbid IQ less than 70)

- Significant alcohol or substance abuse within 6 months prior to study entry

- Inability to complete research measures in English

- Any condition that may make risperidone use medically inadvisable