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临床试验/NCT03076346
NCT03076346已完成不适用

Neural Biomarkers of Clozapine Response

University of Pittsburgh1 个研究点 分布在 1 个国家目标入组 41 人开始时间: 2017年9月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
41
试验地点
1
主要终点
Changes in resting state functional connectivity with efficacious clozapine treatment

研究概览

简要总结

Clozapine has consistently shown to be a superior drug for psychosis in patients who do not respond to other treatments, but its mechanism of action remains unknown. The overall goal of this study is to examine the functional neural circuitry that underlies successful treatment with clozapine, which may lead to the identification of biomarkers that will allow for more efficient use of clozapine, as well as additional treatment targets for patients with refractory illness.

详细描述

A large number of patients with chronic psychotic disorders continue to have symptoms following unsuccessful trials with first-line antipsychotic drugs. For these patients with refractory psychosis, clozapine has consistently demonstrated superior efficacy. Clozapine is often underutilized and administered late in a patient's course of treatment, which leads to increased morbidity, unnecessary medication trials, and increased health care expenditure. Meanwhile, the mechanism of action underlying clozapine's novel effects remains unknown and has not been studied with modern neuroimaging methods. Identifying the neural mechanisms by which clozapine exerts its effects may lead to biomarkers that will facilitate efficient utilization of the drug, and introduce novel treatment targets. In patients with refractory psychotic symptoms, the proposed study will use resting-state and task-based functional MRI (fMRI) to examine the neural circuitry of efficacious treatment with a trial of clozapine. Patients will undergo fMRI scanning both before and after 12 weeks of treatment, with the aims of determining: baseline patterns of resting-state functional connectivity and task-based activation that predict response to treatment; and changes in resting-state and task-based functional circuitry associated with efficacious treatment. Results of this proposal may lead to biomarkers that will optimize treatment algorithms for psychotic disorders and facilitate drug development for refractory psychosis.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 50 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Current positive symptoms rated ≥4 (moderate) on one or more of these Brief Psychiatric Rating Scale items: hallucinatory behavior, unusual thought content and conceptual disorganization.
  • Patient has failed two trials of treatment with antipsychotic drugs and the patient's clinical team is initiating clozapine.
  • Age of 18 to
  • Patient is competent and willing to sign informed consent.
  • For female patients, negative pregnancy test and agreement to use a medically accepted birth control method.
  • Diagnosis of schizophrenia or schizoaffective disorder

排除标准

  • Serious neurological or endocrine disorder.
  • Any medical condition which requires treatment with a medication with psychotropic effects
  • Significant risk of suicidal or homicidal behavior
  • Cognitive or language limitations, or any other factor that would preclude subjects providing informed consent
  • Contraindications to treatment with clozapine (e.g. failed response in past, or history of adverse reactions to treatment).
  • Contraindications to magnetic resonance imaging (e.g. pacemaker).
  • Female patients who are pregnant or breast feeding.

结局指标

主要结局

Changes in resting state functional connectivity with efficacious clozapine treatment

时间窗: 12 weeks

The investigators will examine the functional circuitry associated with a reduction of psychotic symptoms assessed with the Brief Psychiatric Rating Scale.

次要结局

  • Baseline prediction of clozapine response(12 weeks)

研究者

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

Deepak K. Sarpal, M.D.

MD

University of Pittsburgh

研究点 (1)

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