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临床试验/NCT00362804
NCT00362804已完成不适用

Augmentation of Antipsychotic Partial Responders With Tetrabenazine

Centre for Addiction and Mental Health2 个研究点 分布在 1 个国家目标入组 41 人开始时间: 2002年2月1日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
41
试验地点
2
主要终点
BPRS

研究概览

简要总结

Purpose of Study:

A) To improve outcome in large population of antipsychotic patients with schizophrenia or schizoaffective who are only partial responders B) To increase understanding of pharmacology and mechanisms of action underlying antipsychotic effect

Hypothesis/Objectives of the Study:

Tetrabenazine, through its pre-synaptic action, should augment the post-synaptic effects of an antipsychotic.

Background and Rationale for the study:

Preliminary evidence that other amine-depleting agents e.g., reserpine, can induce such an effect

详细描述

Since the 1950's, antipsychotics have been used as the mainstay treatment to control symptoms of schizophrenia. However, soon after their introduction it became apparent that a substantial number of individuals show a less than optimal response to these drugs - as many as 30% of schizophrenics using conventional antipsychotics derive little benefit. Furthermore, 'atypical' generation antipsychotics such as clozapine which proves to be the most beneficial for partial responders and represents the cornerstone of treatment-resistant schizophrenia, offers a response rate as low as 30% in those showing an inadequate response. Moreover, many individuals decline clozapine as an option, or cannot tolerate it.

For these reasons, augmentation strategies play an important role in the treatment of antipsychotic partial responders. We have systematically reviewed the different augmentation options, and reached the conclusion that most such strategies are theoretically speculative and empirically unsupported.

At the same time though, we recognize that augmentation strategies are common practice in the clinical setting. With so many individuals showing only a partial response to antipsychotic treatment (typical or atypical), it has become a practical reality in efforts to offer further improvement. Often, this come in the form of adding one or even more antipsychotics, although the evidence for such an approach is less than compelling and neuroimaging from our centre has cautioned against this approach.

With a variety of other potential augmentation strategies available, we have chosen to focus on tetrabenazine (TBZ), which is currently licensed here in Canada for the management of hyperkinetic movement disorders.

The choice of TBZ as an augmentation strategy arises from several lines of investigation:

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • has been on an antipsychotic medication for at least 3 months and achieved the maximum dose vis à vis tolerability/side effects.
  • Partial response to antipsychotic medication (CGI > 4; BPRS [Anchored, 18-item] total > 30; single item score > 4 on 2 positive symptom items)
  • has been on at least 2 previous antipsychotic trials of 4-6 weeks in duration at a dose reaching 400-600 mg chlorpromazine (or equivalent) with no clinical improvement

排除标准

  • age < 18 or > 65
  • previous documentation of hypersensitivity to tetrabenazine
  • SCID criteria for a current depressive episode
  • MAOI administration within 2 weeks of tetrabenazine treatment
  • concomitant desipramine use
  • diagnosis of idiopathic Parkinson's disease and/or levodopa treatment
  • current unstable medical illness and current substance abuse

结局指标

主要结局

BPRS

时间窗: weekly assessments

CGI

时间窗: weekly assessment

次要结局

  • SAS(weekly)
  • BAS(weeekly)
  • AIMS(weekly)
  • UKU (a general measure of adverse effects)(weekly)
  • GAF/NOISE(weekly)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Gary Remington

Principal Investigator

Centre for Addiction and Mental Health

研究点 (2)

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