search
Back to results

Clozapine IM and Aggression in Schizophrenic Patients

Primary Purpose

Schizophrenia

Status
Withdrawn
Phase
Phase 3
Locations
Israel
Study Type
Interventional
Intervention
clozapine
haloperidol
Sponsored by
Beersheva Mental Health Center
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Schizophrenia focused on measuring schizophrenia, aggression, clozapine, efficacy, double-blind

Eligibility Criteria

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

Inclusion Criteria: schizophrenic, schizoaffective, or schizophreniform according to DSM-IV treatment-resistant presenting pathologic violent-aggressive behavior on admission at risk for self damage age: 18-65 patient is not participating in any other study at time of this study minimal score of 70 on PANSS prior resistance to at least 2 different classes of neuroleptics OAS scores of at least 4 points in physical aggression sections and at least 2 points in verbal aggression section Exclusion Criteria: neutropenia or any other abnormal CBC result myeloproliferative disease chronic physical diseases such as liver, renal or cardiac diseases history of alcohol or drug abuse history of drug induced granulocytopenia/agranulocytosis alcoholic/drug psychosis or intoxication carbamazepine or other bone marrow suppressor treatment uncontrolled epilepsy paralytic ileus hypersensitivity to clozapine

Sites / Locations

  • Beersheva Mental Health Center
  • Nes Ziona Medical Center

Outcomes

Primary Outcome Measures

Positive and Negative Syndrome Scale
Overt Aggression Scale

Secondary Outcome Measures

Full Information

First Posted
September 11, 2005
Last Updated
July 23, 2013
Sponsor
Beersheva Mental Health Center
search

1. Study Identification

Unique Protocol Identification Number
NCT00189995
Brief Title
Clozapine IM and Aggression in Schizophrenic Patients
Official Title
Intramuscular Clozapine in the Management of Aggression in Schizophrenic Patients
Study Type
Interventional

2. Study Status

Record Verification Date
October 2005
Overall Recruitment Status
Withdrawn
Study Start Date
undefined (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
undefined (undefined)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Beersheva Mental Health Center

4. Oversight

5. Study Description

Brief Summary
Aggressive, persistent aggression and impulsive behavior are frequently observed in schizophrenic patients. According to some researchers "more than 50% of all psychiatric patients and 10% of schizophrenic patients show aggressive symptoms varying from threatening behavior and agitation to assault"(1). It is a common cause of psychiatric admission and is a therapeutic issue. The treatment of these symptoms is a clinical problem for both patients and staff. Violent behavior, a major detrimental factor in stigmatization of the mentally ill, also poses physical danger for the patients themselves. Current pharmacotherapy of pathologic aggression involves the use of multiple agents (typical and atypical antipsychotics, benzodiazepines, mood stabilizers, beta-blockers, antiandrogenic hormones, and selective serotonin reuptake inhibitors) on empiric basis, with varying degrees of response (2-6). Unfortunately, these approaches lead to numerous side effects. Poor or noncompliance with pharmacotherapy makes it difficult to choose the appropriate preparation. Currently, typical neuroleptics are still the first choice in treating acute aggressive symptoms, while risperidone and olanzapine could be alternatives (5-7). Typical depot neuroleptics should be considered in cases where medication compliance is a problem. Most clinical information on treating of aggression has been collected about atypical neuroleptics, particularly regarding clozapine. Clozapine is indicated in psychotic state and/or in drug-resistant schizophrenic patients. According to the FDA - it is the drug of choice in suicidal and aggressive patients, due-to psychotic state. It was found helpful in nearly 30% of resistant schizophrenic patients. Concerning the parenteral administration of clozapine - very little data is available today. This study aims to investigate efficacy and safety (psychopathology, and side effects) of parenteral clozapine in treatment of aggressive behavior in schizophrenic patients in a double-blind trial.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Schizophrenia
Keywords
schizophrenia, aggression, clozapine, efficacy, double-blind

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
Double
Allocation
Randomized
Enrollment
0 (Actual)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
clozapine
Intervention Type
Drug
Intervention Name(s)
haloperidol
Primary Outcome Measure Information:
Title
Positive and Negative Syndrome Scale
Title
Overt Aggression Scale

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: schizophrenic, schizoaffective, or schizophreniform according to DSM-IV treatment-resistant presenting pathologic violent-aggressive behavior on admission at risk for self damage age: 18-65 patient is not participating in any other study at time of this study minimal score of 70 on PANSS prior resistance to at least 2 different classes of neuroleptics OAS scores of at least 4 points in physical aggression sections and at least 2 points in verbal aggression section Exclusion Criteria: neutropenia or any other abnormal CBC result myeloproliferative disease chronic physical diseases such as liver, renal or cardiac diseases history of alcohol or drug abuse history of drug induced granulocytopenia/agranulocytosis alcoholic/drug psychosis or intoxication carbamazepine or other bone marrow suppressor treatment uncontrolled epilepsy paralytic ileus hypersensitivity to clozapine
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Valdimir Lerner, MD, PhD
Organizational Affiliation
Ben-Gurion University of the Negev
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Baruch Spivak, MD
Organizational Affiliation
Tel Aviv University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Chanoch Midownik, MD
Organizational Affiliation
Ben-Gurion University of the Negev
Official's Role
Principal Investigator
Facility Information:
Facility Name
Beersheva Mental Health Center
City
Beersheva
Country
Israel
Facility Name
Nes Ziona Medical Center
City
Nes Ziona
Country
Israel

12. IPD Sharing Statement

Learn more about this trial

Clozapine IM and Aggression in Schizophrenic Patients

We'll reach out to this number within 24 hrs