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Olanzapine Versus Clozapine in Treatment Refractory Schizophrenia

Primary Purpose

Schizophrenia, Schizoaffective Disorder

Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
olanzapine vs. clozapine
Sponsored by
Vanderbilt University
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Schizophrenia

Eligibility Criteria

18 Years - 60 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Patients will be males and females, ages 18-60, with a definite diagnosis by DSM-IV criteria of schizophrenia (any subtype) or schizoaffective disorder. 2) All participants will be refractory according to the Kane et al (1988) criteria, with modification on the number of drug trials to at least two neuroleptic drugs at adequate doses for periods > 3 months. The criteria of Kane et al. for treatment resistance are as follows: three or more trials with antipsychotic drugs of adequate dose and duration (this is usually 4-6 weeks). The original criteria involved three types of typical neuroleptic drugs. Now, it can include any antipsychotic drug other than clozapine. Olanzapine may have been tried but the dose must not have exceeded 30 mg/day. Subjects must have a PANNS-derived BPRS total score > 24 (0-6 scale) or BPRS positive subscale item score > 3 on at least two of the four items. Participants will be in generally good and stable physical health. Written informed consent will be obtained from all participants after a full explanation of the study and procedures. For those patients with a legal guardian, written informed consent will be obtained from the guardian, with verbal assent by the research subject. Since both clozapine and olanzapine are approved agents, no specific birth control will be required for females, but advice about birth control will be provided Exclusion Criteria: Uncontrolled diabetes or hypertension. Cardiac conduction abnormality or uncontrolled arrhythmia. History of any blood dyscrasia, including leukemia. Significant active hepatic or renal disease, including chronic hepatitis. Clinically significant neurological disorder, including (but not limited to) Parkinson's disease, multiple sclerosis, seizure disorder, intracranial mass lesion (note that the presence of tardive dyskinesia is not an exclusion for participants). Active cancer with or without chemotherapy within the last five years (not to include a completely excised basal cell carcinoma). Active endocrinological disorder (which does not include adequately treated hypothyroidism). Pregnancy or lactation. An active substance use disorder within the last six months. History of lack of response to an adequate trial of monotherapy with either clozapine or olanzapine in which the dose of clozapine must be > 600 mg/day or the dose of olanzapine must be > 20 mg/day; and the duration of treatment with either must be > 6 weeks. History of intolerance of clozapine or olanzapine, including blood dyscrasia

Sites / Locations

    Outcomes

    Primary Outcome Measures

    There has not been an adequate of test of whether olanzapine is as effective as clozapine in treatment
    resistant patients. Several recent studies suggest olanzapine may be effective in some clozapine responders as well as in treatment resistant patients. A head to head comparison is needed to clarify the relative efficacy

    Secondary Outcome Measures

    Full Information

    First Posted
    September 13, 2005
    Last Updated
    September 13, 2005
    Sponsor
    Vanderbilt University
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    1. Study Identification

    Unique Protocol Identification Number
    NCT00179231
    Brief Title
    Olanzapine Versus Clozapine in Treatment Refractory Schizophrenia
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    September 2005
    Overall Recruitment Status
    Completed
    Study Start Date
    May 2000 (undefined)
    Primary Completion Date
    undefined (undefined)
    Study Completion Date
    February 2004 (undefined)

    3. Sponsor/Collaborators

    Name of the Sponsor
    Vanderbilt University

    4. Oversight

    5. Study Description

    Brief Summary
    The study involves a six-month, double-blind protocol during which eighty patients, across three sites around the country, will be randomly assigned to receive clozapine or olanzapine. The specific aims of the study are to evaluate the relative effects of olanzapine and clozapine on clinical outcomes and cognition in patients diagnosed with schizophrenia or schizoaffective disorder who have demonstrated resistance to treatment in the past.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Schizophrenia, Schizoaffective Disorder

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    Double
    Allocation
    Randomized
    Enrollment
    80 (false)

    8. Arms, Groups, and Interventions

    Intervention Type
    Drug
    Intervention Name(s)
    olanzapine vs. clozapine
    Primary Outcome Measure Information:
    Title
    There has not been an adequate of test of whether olanzapine is as effective as clozapine in treatment
    Title
    resistant patients. Several recent studies suggest olanzapine may be effective in some clozapine responders as well as in treatment resistant patients. A head to head comparison is needed to clarify the relative efficacy

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    60 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Patients will be males and females, ages 18-60, with a definite diagnosis by DSM-IV criteria of schizophrenia (any subtype) or schizoaffective disorder. 2) All participants will be refractory according to the Kane et al (1988) criteria, with modification on the number of drug trials to at least two neuroleptic drugs at adequate doses for periods > 3 months. The criteria of Kane et al. for treatment resistance are as follows: three or more trials with antipsychotic drugs of adequate dose and duration (this is usually 4-6 weeks). The original criteria involved three types of typical neuroleptic drugs. Now, it can include any antipsychotic drug other than clozapine. Olanzapine may have been tried but the dose must not have exceeded 30 mg/day. Subjects must have a PANNS-derived BPRS total score > 24 (0-6 scale) or BPRS positive subscale item score > 3 on at least two of the four items. Participants will be in generally good and stable physical health. Written informed consent will be obtained from all participants after a full explanation of the study and procedures. For those patients with a legal guardian, written informed consent will be obtained from the guardian, with verbal assent by the research subject. Since both clozapine and olanzapine are approved agents, no specific birth control will be required for females, but advice about birth control will be provided Exclusion Criteria: Uncontrolled diabetes or hypertension. Cardiac conduction abnormality or uncontrolled arrhythmia. History of any blood dyscrasia, including leukemia. Significant active hepatic or renal disease, including chronic hepatitis. Clinically significant neurological disorder, including (but not limited to) Parkinson's disease, multiple sclerosis, seizure disorder, intracranial mass lesion (note that the presence of tardive dyskinesia is not an exclusion for participants). Active cancer with or without chemotherapy within the last five years (not to include a completely excised basal cell carcinoma). Active endocrinological disorder (which does not include adequately treated hypothyroidism). Pregnancy or lactation. An active substance use disorder within the last six months. History of lack of response to an adequate trial of monotherapy with either clozapine or olanzapine in which the dose of clozapine must be > 600 mg/day or the dose of olanzapine must be > 20 mg/day; and the duration of treatment with either must be > 6 weeks. History of intolerance of clozapine or olanzapine, including blood dyscrasia
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Herbert Y Meltzer, M.D.
    Organizational Affiliation
    Vanderbilt University Medical Center
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Citations:
    PubMed Identifier
    18232726
    Citation
    Meltzer HY, Bobo WV, Roy A, Jayathilake K, Chen Y, Ertugrul A, Anil Yagcioglu AE, Small JG. A randomized, double-blind comparison of clozapine and high-dose olanzapine in treatment-resistant patients with schizophrenia. J Clin Psychiatry. 2008 Feb;69(2):274-85. doi: 10.4088/jcp.v69n0214.
    Results Reference
    derived

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    Olanzapine Versus Clozapine in Treatment Refractory Schizophrenia

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