Clozapine Versus Other Atypical Antipsychotics for Bipolar Disorder
Primary Purpose
Bipolar Disorder
Status
Unknown status
Phase
Phase 4
Locations
Brazil
Study Type
Interventional
Intervention
Clozapine
Risperidone
Olanzapine
Quetiapine
Sponsored by
About this trial
This is an interventional treatment trial for Bipolar Disorder
Eligibility Criteria
Inclusion Criteria:
- DSM-IV Bipolar I Disorder;
- having had a mood episode within the preceding year; DSM-IV rapid cyclers will be permitted to participate in this study;
- males or females between 18 and 65 years of age;
- ongoing illness symptoms including significant functional impairment;
- documented history of treatment resistance, defined as persistent symptoms despite simultaneous, adequate treatment with at least two medications: one mood stabilizer (lithium or valproate) + antipsychotic OR two mood stabilizers (at least one of them being lithium or valproate).
- each patient must have a level of understanding sufficient to agree to all the tests required by the protocol and must sign an informed consent document
Exclusion Criteria:
- patients with onset of illness after age 40 or illness resulting from secondary causes
- women who are pregnant or breastfeeding, or not using adequate contraception
- unstable medical illnesses
- clinically significant abnormal laboratory tests
- current active alcohol or substance abuse
- severe personality disorders
- contraindication to the use of clozapine or previous treatment with clozapine
Sites / Locations
- Hospital de Clínicas de Porto AlegreRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Clozapine
Risperidone, olanzapine or quetiapine
Arm Description
Clozapine, P.O., flexible dose, for up to 6 months
Risperidone, olanzapine or quetiapine, according to clinical indication, flexible dose, for up to 6 months
Outcomes
Primary Outcome Measures
Functioning according to Functioning Assessment Short-Test
Global functioning according to Functioning Assessment Short-Test
Secondary Outcome Measures
Time to all-cause treatment failure
Include drug treatment (commencement of a new drug, restarting of a discontinued drug, or increasing the investigational drug dose in response to an emergent mood episode), admission to hospital or withdrawal from study treatment.
Full Information
NCT ID
NCT02562287
First Posted
August 11, 2015
Last Updated
October 1, 2018
Sponsor
Hospital de Clinicas de Porto Alegre
Collaborators
Coordenação de Aperfeiçoamento de Pessoal de Nível Superior., Conselho Nacional de Desenvolvimento Científico e Tecnológico
1. Study Identification
Unique Protocol Identification Number
NCT02562287
Brief Title
Clozapine Versus Other Atypical Antipsychotics for Bipolar Disorder
Official Title
A Randomized Controlled Trial to Evaluate the Effectiveness of Clozapine Versus Olanzapine, Quetiapine or Risperidone in Treatment Resistant Bipolar Disorder
Study Type
Interventional
2. Study Status
Record Verification Date
October 2018
Overall Recruitment Status
Unknown status
Study Start Date
October 2015 (undefined)
Primary Completion Date
June 2019 (Anticipated)
Study Completion Date
December 2020 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Hospital de Clinicas de Porto Alegre
Collaborators
Coordenação de Aperfeiçoamento de Pessoal de Nível Superior., Conselho Nacional de Desenvolvimento Científico e Tecnológico
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The clinical use of clozapine has been an unequivocal advance in the treatment of schizophrenia, a chronic and severe mental illness. A wealth of clinical data demonstrates it offers enhanced efficacy on both positive and negative symptomatology, improving cognition, functioning and quality of life. It is also associated with improved compliance and a continued efficacy in long-term treatment that can be translated into a reduction of suicidality and all-cause mortality. Because of preclinical evidence that it modulates neuroplasticity and prefrontal cortex connectivity, clozapine may be an interesting strategy for further severe psychotic illnesses. Nevertheless, even considering the growing use of other atypical antipsychotics in the management of bipolar disorder, a role for clozapine has been poorly defined. The clinical evidence-base for its use in this condition is largely based on uncontrolled naturalistic trials and retrospective studies and chart reviews. Several of these have supported clozapine's efficacy in treatment-resistant bipolar disorder. Possibly because of clozapine's profile of adverse effects and lack of interest from pharmaceutical companies, only two randomized trials have examined its effectiveness. Both suggest clinically relevant antimanic and mood-stabilizing properties. Therefore, the primary objective of this trial is to determine the effectiveness of clozapine for treatment-resistant bipolar disorder. Secondary objectives include examining the effects of treatment with clozapine on cognition and functioning of patients with bipolar disorder. Tolerability and safety of long-term clozapine use will also be examined. To that end, the investigators will conduct a clinical trial with 54 patients with a history of treatment resistance. Patients will be randomized to either open-label treatment with clozapine, in combination with lithium or valproate, or open-label treatment with an atypical antipsychotic with consistent evidence of efficacy in the treatment of bipolar disorder (olanzapine, quetiapine or risperidone), also in combination with lithium or valproate. Patients will be followed for one-year and time to all-cause treatment failure will be the primary outcome measure. It is the belief of the investigators that this study will generate meaningful clinical data of tremendous importance to validate clozapine as a legitimate treatment option for treatment-resistant bipolar disorder.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bipolar Disorder
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
54 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Clozapine
Arm Type
Experimental
Arm Description
Clozapine, P.O., flexible dose, for up to 6 months
Arm Title
Risperidone, olanzapine or quetiapine
Arm Type
Active Comparator
Arm Description
Risperidone, olanzapine or quetiapine, according to clinical indication, flexible dose, for up to 6 months
Intervention Type
Drug
Intervention Name(s)
Clozapine
Other Intervention Name(s)
Clozaril
Intervention Description
Flexible dosage, with up-titration according to standard schedules employed for schezophrenia
Intervention Type
Drug
Intervention Name(s)
Risperidone
Other Intervention Name(s)
Risperdal
Intervention Description
Risperidone, in a flexible dosage
Intervention Type
Drug
Intervention Name(s)
Olanzapine
Other Intervention Name(s)
Zyprexa
Intervention Description
Olanzapine, flexible dosage
Intervention Type
Drug
Intervention Name(s)
Quetiapine
Other Intervention Name(s)
Seroquel
Intervention Description
Quetiapine, flexible dosage
Primary Outcome Measure Information:
Title
Functioning according to Functioning Assessment Short-Test
Description
Global functioning according to Functioning Assessment Short-Test
Time Frame
6 month follow up
Secondary Outcome Measure Information:
Title
Time to all-cause treatment failure
Description
Include drug treatment (commencement of a new drug, restarting of a discontinued drug, or increasing the investigational drug dose in response to an emergent mood episode), admission to hospital or withdrawal from study treatment.
Time Frame
Six 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:
DSM-IV Bipolar I Disorder;
having had a mood episode within the preceding year; DSM-IV rapid cyclers will be permitted to participate in this study;
males or females between 18 and 65 years of age;
ongoing illness symptoms including significant functional impairment;
documented history of treatment resistance, defined as persistent symptoms despite simultaneous, adequate treatment with at least two medications: one mood stabilizer (lithium or valproate) + antipsychotic OR two mood stabilizers (at least one of them being lithium or valproate).
each patient must have a level of understanding sufficient to agree to all the tests required by the protocol and must sign an informed consent document
Exclusion Criteria:
patients with onset of illness after age 40 or illness resulting from secondary causes
women who are pregnant or breastfeeding, or not using adequate contraception
unstable medical illnesses
clinically significant abnormal laboratory tests
current active alcohol or substance abuse
severe personality disorders
contraindication to the use of clozapine or previous treatment with clozapine
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
PEDRO V MAGALHAES, M.D., Ph.D.
Phone
+555191123773
Email
pedromaga2@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
PEDRO V MAGALHAES, M.D., Ph.D.
Organizational Affiliation
Hospital de Clínicas de Porto Alegre / Universidade Federal do Rio Grande do Sul
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hospital de Clínicas de Porto Alegre
City
Porto Alegre
State/Province
Rio Grande Do Sul
ZIP/Postal Code
90540001
Country
Brazil
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
PEDRO V MAGALHAES, M.D., Ph.D.
12. IPD Sharing Statement
Learn more about this trial
Clozapine Versus Other Atypical Antipsychotics for Bipolar Disorder
We'll reach out to this number within 24 hrs