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Clozapine Versus Amisulpride in Treatment-resistant Schizophrenia Patients (ClozAmi)

Primary Purpose

Schizophrenia, Treatment Resistant Disorders

Status
Withdrawn
Phase
Not Applicable
Locations
Israel
Study Type
Interventional
Intervention
Clozapine
Amisulpride
Clozapine+Amisulpride
Sponsored by
Geha Mental Health Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Schizophrenia focused on measuring schizophrenia, clozapine, amisulpride, combination, treatment resistant

Eligibility Criteria

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

Inclusion Criteria:

  1. Confirmed diagnosis of schizophrenia according to DSM-IV-TR criteria
  2. Treatment-resistant schizophrenia, defined as: documented treatment failure (insufficient clinical response or severe adverse effects) of two antipsychotics (one of them should be atypical) for an adequate duration of 6 weeks and in a sufficient dose of at least 600 mg/day of chlorpromazine equivalent
  3. Age 18-65 years
  4. Basal PANSS > 75
  5. CGI-S >3
  6. Persistent positive psychotic symptoms, with rating scores of moderate or worse on at least two of four positive symptom items (delusions, conceptual disorganization, hallucinatory behavior, and suspiciousness/persecution) on Positive and Negative Syndrome Scale (PANSS).
  7. Competent and willing to provide written, informed consent

Exclusion Criteria:

  1. Patients with concomitant treatment with lithium, anticonvulsants, antidepressants
  2. Patients with underlying severe medical illness, such as cardiovascular disease, cerebrovascular disease, bone marrow suppression or epilepsy
  3. A previous trial of clozapine or amisulpride
  4. Any known contraindication for treatment with clozapine or amisulpride
  5. Any woman who is pregnant or planning a pregnancy, and any woman of child bearing potential unless using adequate contraception

Sites / Locations

  • Geha Mental Health Center

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Experimental

Arm Label

Clozapine

Amisulpride

Augmentation

Arm Description

Clozapine monotherapy

Amisulpride monotherapy

Augmentation of clozapine with amisulpride

Outcomes

Primary Outcome Measures

Change from baseline in Positive and Negative Syndrome Scale (PANSS)

Secondary Outcome Measures

Change from baseline in Clinical Global Impression - Severity (CGI-S)
Change from baseline in Beck Depression Inventory (BDI)
Change from baseline in Beck Anxiety Inventory (BAI)
Change from baseline in Schizophrenia Quality of Life Scale (SQLS)
Change from baseline in Simpson-Angus Scale (SAS)
Change from baseline in Clozapine Adverse Effects Inventory (CAEI)

Full Information

First Posted
October 2, 2011
Last Updated
December 8, 2015
Sponsor
Geha Mental Health Center
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1. Study Identification

Unique Protocol Identification Number
NCT01448499
Brief Title
Clozapine Versus Amisulpride in Treatment-resistant Schizophrenia Patients
Acronym
ClozAmi
Official Title
Clozapine Versus Amisulpride Versus Their Combination in the Treatment of Drug-resistant Schizophrenia Patients
Study Type
Interventional

2. Study Status

Record Verification Date
December 2015
Overall Recruitment Status
Withdrawn
Study Start Date
October 2011 (undefined)
Primary Completion Date
October 2013 (Anticipated)
Study Completion Date
undefined (undefined)

3. Sponsor/Collaborators

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

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Background: schizophrenia is a debilitating mental disorder affecting about 1% of the general population. About 30% of patients will not react to current drug treatment and defined as treatment-resistant schizophrenia patients (TRSP). The best studied therapeutic option for this population is clozapine therapy. Clozapine was shown to be effective than any other antipsychotic drug in TRSP. Moreover, augmentation of clozapine was not demonstrated to be more effective than clozapine monotherapy. Albeit Clozapine superiority in TRSP, its use may be involved with many adverse effects, some of them are life-threatening, and need for routine blood tests. Amisulpride is an atypical antipsychotic drug with a different mechanism of action than clozapine, with less adverse effects. No study compared directly amisulpride and clozapine in TRSP. Study objective: to compare, for the first time, the broad clinical effectiveness of clozapine and amisulpride and their combination in TRSP. Study Design: a clinical, prospective, naturalistic, randomized, comparative study simulating a real-world approach of clinical decision making. Methods: a total of 140 TRSP will be recruited from a large regional mental health center. Participants will be randomized into two treatment groups (70 in each group): clozapine monotherapy and amisulpride monotherapy. Assessment will be done following 10 and 20 weeks of treatment. In case of treatment failure (insufficient clinical response or severe adverse effect) participants will be offered either to switch to clozapine treatment (for failed amisulpride treatment) or to augment clozapine with amisulpride (for failed clozapine monotherapy patients). Thereafter, participants will be followed-up for a year. Assessment will be made using clinician rated scales and self-completed questionnaires, rating the broad phenomenology of schizophrenia (psychosis, mood, anxiety, obsessive-compulsive, cognitive and quality of life) and drug-related adverse effects (objective and subjective). Analysis: comparison of the effectiveness of the three treatment groups: amisulpride, clozapine and their combination, in the various dimensions of TRSP.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Schizophrenia, Treatment Resistant Disorders
Keywords
schizophrenia, clozapine, amisulpride, combination, treatment resistant

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
0 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Clozapine
Arm Type
Experimental
Arm Description
Clozapine monotherapy
Arm Title
Amisulpride
Arm Type
Experimental
Arm Description
Amisulpride monotherapy
Arm Title
Augmentation
Arm Type
Experimental
Arm Description
Augmentation of clozapine with amisulpride
Intervention Type
Drug
Intervention Name(s)
Clozapine
Intervention Description
escalating dose of clozapine up to 900 mg/day
Intervention Type
Drug
Intervention Name(s)
Amisulpride
Intervention Description
escalating dose of amisulpride up to 800 mg/day
Intervention Type
Drug
Intervention Name(s)
Clozapine+Amisulpride
Intervention Description
augmentation of clozapine with amisulpride
Primary Outcome Measure Information:
Title
Change from baseline in Positive and Negative Syndrome Scale (PANSS)
Time Frame
10, 20 weeks and endpoint
Secondary Outcome Measure Information:
Title
Change from baseline in Clinical Global Impression - Severity (CGI-S)
Time Frame
10 , 20 weeks and endpoint
Title
Change from baseline in Beck Depression Inventory (BDI)
Time Frame
10 , 20 weeks and endpoint
Title
Change from baseline in Beck Anxiety Inventory (BAI)
Time Frame
10, 20 weeks and endpoint
Title
Change from baseline in Schizophrenia Quality of Life Scale (SQLS)
Time Frame
10, 20 weeks and endpoint
Title
Change from baseline in Simpson-Angus Scale (SAS)
Time Frame
5, 10, 15, 20 weeks, endpoint
Title
Change from baseline in Clozapine Adverse Effects Inventory (CAEI)
Time Frame
5, 10 ,15, 20 weeks, endpoint

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: Confirmed diagnosis of schizophrenia according to DSM-IV-TR criteria Treatment-resistant schizophrenia, defined as: documented treatment failure (insufficient clinical response or severe adverse effects) of two antipsychotics (one of them should be atypical) for an adequate duration of 6 weeks and in a sufficient dose of at least 600 mg/day of chlorpromazine equivalent Age 18-65 years Basal PANSS > 75 CGI-S >3 Persistent positive psychotic symptoms, with rating scores of moderate or worse on at least two of four positive symptom items (delusions, conceptual disorganization, hallucinatory behavior, and suspiciousness/persecution) on Positive and Negative Syndrome Scale (PANSS). Competent and willing to provide written, informed consent Exclusion Criteria: Patients with concomitant treatment with lithium, anticonvulsants, antidepressants Patients with underlying severe medical illness, such as cardiovascular disease, cerebrovascular disease, bone marrow suppression or epilepsy A previous trial of clozapine or amisulpride Any known contraindication for treatment with clozapine or amisulpride Any woman who is pregnant or planning a pregnancy, and any woman of child bearing potential unless using adequate contraception
Facility Information:
Facility Name
Geha Mental Health Center
City
Petach-Tikva
ZIP/Postal Code
49000
Country
Israel

12. IPD Sharing Statement

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Clozapine Versus Amisulpride in Treatment-resistant Schizophrenia Patients

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