Preventing Morbidity in First-Episode Schizophrenia
Trial Snapshot
- Phase
- Phase 4
- Status
- Completed
- Sponsor
- Northwell Health
- Enrollment
- 125
- Locations
- 4
- Primary Endpoint
- Treatment response
Study Overview
Brief Summary
This 3-year study will determine if the antipsychotic medications olanzapine (Zyprexa®) and risperidone (Risperdal®) can help patients with first-episode schizophrenia.
Detailed Description
The goal of the study is to prevent morbidity in first-episode schizophrenia using second-generation antipsychotic drugs: olanzapine, risperidone.
Long-term studies of first-episode schizophrenia patients have clearly indicated excellent initial responsiveness of positive psychotic symptoms to treatment with conventional antipsychotic medications. However, in the years immediately following this initial good response, morbidity increases. Relapses, often multiple ones, are the rule and are usually precipitated by medication noncompliance. There is some evidence that the second-generation antipsychotic drugs may have superior efficacy in terms of these outcome domains. However, these newer agents have been studied primarily in chronic and/or treatment-resistant patient samples and there are virtually no long-term studies or studies comparing the new drugs with one another.
First episode patients are randomly assigned to treatment with olanzapine or risperidone for 3 years. Outcome measures for the initial episode include psychopathology (positive, negative, and affective symptoms), side effects, neurocognition (executive function, memory, and attention), social and occupational function and service utilization. The effects on long-term course are measured in terms of frequency and timing of relapses, level of recovery from subsequent episodes and prospectively assessed course of psychopathology, neurocognitive function, social/vocational function, and service utilization.
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Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Treatment
- Masking
- Single (Outcomes Assessor)
Eligibility Criteria
- Ages
- 16 Years to 40 Years (Child, Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •First episode schizophrenia, schizophreniform disorder or schizoaffective disorder
Exclusion Criteria
- •Prior treatment with antipsychotic medications.
Outcomes
Primary Outcomes
Treatment response
Time Frame: 8 consecutive weeks
Secondary Outcomes
No secondary outcomes reported
Investigators
Delbert Robinson
Delbert Robinson, MD/Prinicipal Investigator
National Institute of Mental Health (NIMH)
