search
Back to results

A Study of the Effects of Risperidone and Olanzapine on Blood Glucose (Sugar) in Patients With Schizophrenia or Schizoaffective Disorder

Primary Purpose

Schizophrenia, Diabetes Mellitus

Status
Completed
Phase
Phase 4
Locations
Study Type
Interventional
Intervention
Olanzapine
Risperidone
Sponsored by
Janssen, LP
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Schizophrenia focused on measuring schizophrenia, blood glucose, glucose metabolism, diabetes mellitus, risperidone, olanzapine

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Diagnosis of schizophrenia or related disorder stable with respect to disease symptoms and other medical conditions would benefit from this type of antipsychotic drug if female, using birth control. Exclusion Criteria: Patients who are delirious, bipolar, severely mentally retarded, or suicidal psychiatric diagnosis of disease unrelated to schizophrenia presence of stroke, brain tumor, Parkinson's Disease, or diseases that affect blood glucose control history of diabetes long or recent history of taking risperidone, olanzapine, quetiapine, clozapine, or investigational drugs recent history of unstable thyroid function if female, not using birth control abusing drugs or alcohol.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Experimental

    Arm Label

    001

    002

    Arm Description

    Risperidone Target oral dose of 6 milligrams per day for for 6 months

    Olanzapine Target oral dose of 20 milligrams per day for 6 months

    Outcomes

    Primary Outcome Measures

    Change in the Disposition Index derived from the Frequently Sampled Intravenous Glucose Tolerance Test (which shows how the body regulates glucose)

    Secondary Outcome Measures

    Changes in measurements of metabolism and glucose regulation; changes in results of tests and questionnaires evaluating the effectiveness and safety (including laboratory tests and anthropomatic measurements) of medications used to treat schizophrenia

    Full Information

    First Posted
    October 7, 2005
    Last Updated
    May 16, 2011
    Sponsor
    Janssen, LP
    search

    1. Study Identification

    Unique Protocol Identification Number
    NCT00236379
    Brief Title
    A Study of the Effects of Risperidone and Olanzapine on Blood Glucose (Sugar) in Patients With Schizophrenia or Schizoaffective Disorder
    Official Title
    A Six-month, Double-blind, Randomized, International, Multicenter Trial to Evaluate the Glucoregulatory Effects of Risperidone and Olanzapine in Subjects With Schizophrenia or Schizoaffective Disorder
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    March 2011
    Overall Recruitment Status
    Completed
    Study Start Date
    undefined (undefined)
    Primary Completion Date
    undefined (undefined)
    Study Completion Date
    August 2003 (Actual)

    3. Sponsor/Collaborators

    Name of the Sponsor
    Janssen, LP

    4. Oversight

    5. Study Description

    Brief Summary
    The purpose of this study is to assess and compare how risperidone and olanzapine, two antipsychotic medications, affect the regulation of glucose (sugar) in the body.
    Detailed Description
    The newer antipsychotic medications risperidone and olanzapine effectively treat schizophrenia and related disorders, and they may cause fewer side effects than the older antipsychotic drugs do. However, some of the newer antipsychotic medications could have a negative effect on the regulation of blood glucose (sugar) in the body. This negative effect could make the patient gain weight and even develop diabetes mellitus. This randomized, double-blind study will assess and compare how risperidone and olanzapine affect the regulation of glucose in the body in patients with schizophrenia and schizoaffective disorder. Patients will be randomly assigned to receive risperidone (target oral dose of 6 milligrams per day) or olanzapine (target oral dose of 20 milligrams per day) for 6 months. Repeat laboratory measurements will be performed and questions will be asked of the patients to evaluate the safety and effectiveness of the drugs. The primary laboratory test used to assess the patient's regulation of blood glucose will be the Disposition Index derived from the Frequently Sampled Intravenous Glucose Tolerance Test. Risperidone 2 milligram oven-encapsulated tablets taken orally once a day for 6 months; olanzapine 5 milligram tablets taken orally once a day for 6 months

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Schizophrenia, Diabetes Mellitus
    Keywords
    schizophrenia, blood glucose, glucose metabolism, diabetes mellitus, risperidone, olanzapine

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 4
    Interventional Study Model
    Parallel Assignment
    Masking
    Double
    Allocation
    Randomized
    Enrollment
    59 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    001
    Arm Type
    Experimental
    Arm Description
    Risperidone Target oral dose of 6 milligrams per day for for 6 months
    Arm Title
    002
    Arm Type
    Experimental
    Arm Description
    Olanzapine Target oral dose of 20 milligrams per day for 6 months
    Intervention Type
    Drug
    Intervention Name(s)
    Olanzapine
    Intervention Description
    Target oral dose of 20 milligrams per day for 6 months
    Intervention Type
    Drug
    Intervention Name(s)
    Risperidone
    Intervention Description
    Target oral dose of 6 milligrams per day for for 6 months
    Primary Outcome Measure Information:
    Title
    Change in the Disposition Index derived from the Frequently Sampled Intravenous Glucose Tolerance Test (which shows how the body regulates glucose)
    Time Frame
    Up to 6 months
    Secondary Outcome Measure Information:
    Title
    Changes in measurements of metabolism and glucose regulation; changes in results of tests and questionnaires evaluating the effectiveness and safety (including laboratory tests and anthropomatic measurements) of medications used to treat schizophrenia
    Time Frame
    Up to 6 months

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    65 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Diagnosis of schizophrenia or related disorder stable with respect to disease symptoms and other medical conditions would benefit from this type of antipsychotic drug if female, using birth control. Exclusion Criteria: Patients who are delirious, bipolar, severely mentally retarded, or suicidal psychiatric diagnosis of disease unrelated to schizophrenia presence of stroke, brain tumor, Parkinson's Disease, or diseases that affect blood glucose control history of diabetes long or recent history of taking risperidone, olanzapine, quetiapine, clozapine, or investigational drugs recent history of unstable thyroid function if female, not using birth control abusing drugs or alcohol.
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Janssen, LP Clinical Trial
    Organizational Affiliation
    Janssen, LP
    Official's Role
    Study Director

    12. IPD Sharing Statement

    Links:
    URL
    http://filehosting.pharmacm.com/DownloadService.ashx?client=CTR_JNJ_6051&studyid=345&filename=CR002758_CSR.pdf
    Description
    A Six-Month, Double Blind, Randomized, International, Multicenter Trial to Evaluate the Glucoregulatory Effects of Risperidone and Olanzapine in Subjects with Schizophrenia or Schizoaffective disorder.

    Learn more about this trial

    A Study of the Effects of Risperidone and Olanzapine on Blood Glucose (Sugar) in Patients With Schizophrenia or Schizoaffective Disorder

    We'll reach out to this number within 24 hrs