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临床试验/EUCTR2010-020579-21-DE
EUCTR2010-020579-21-DE进行中(未招募)不适用

A Phase IV Prospective, Double-blind, Double-dummy, Randomised, Crossover Study to Assess the Impact on Daily Cognitive Functioning of Quetiapine Fumarate Immediate Release (Seroquel IR®) Dosed twice Daily and Quetiapine Fumarate Extended Release (Seroquel XR®) Dosed once Daily in the Evening in Patients with Stable Schizophrenia

AstraZeneca AB0 个研究点目标入组 100 人开始时间: 2010年7月19日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
100

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • 1.Provision of written informed consent prior to any study specific procedures
  • 2.Male and female patients aged 18 and 50 years
  • 3. Documented clinical diagnosis of schizophrenia, paranoid type, for at least 2 years before randomisation meeting the Diagnostic and Statistical Manual of Mental Disorders, 4th Edition, Text Revision (DSM-IV-TR, American Psychiatric Association 2000) criteria of schizophrenia (DSM-IV codes 295.30) confirmed by MINI version 5.0
  • 4. Outpatient status at enrolment
  • 5. 56 days period (8 weeks) of stable psychiatric status before randomisation
  • 6.Treated with quetiapine IR or quetiapine XR in a dose range between 400-750 mg
  • 7.Treated with quetiapine IR or quetiapine XR in a dose range between 400-750 mg
  • 8.Dose of quetiapine IR or quetiapine XR unchanged during the last 56 days before randomisation
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • 1. Diagnosis of any DSM-IV Axis I disorder other than those included in inclusion criteria above within 6 months before randomisation (e.g., alcohol dependence or psychoactive substance dependence not in full remission, concurrent organic mental disorder, or mental retardation [axis II diagnosis]) of a degree that may interfere with the patient’s ability to co-operate.
  • 2. Patients with substance abuse or dependence as defined by DSM-IV-TR criteria and not in full remission or if previous substance abuse or dependence have caused impaired cognition. A urine drug screen test will be performed at enrolment. The investigator will evaluate the toxicology results along with medical history to determine if the patient meets in DSM-IV-TR criteria for substance abuse. Patients are excluded with a single urine toxicology screen (UTS) positive for cocaine, heroin, or PCP
  • 3. Last schizophrenic episode with disorganized (DSM-IV code 295.10), catatonic (DSM-IV code 295.20), residual (DSM-IV code 295.60) type, or undifferentiated type (295.90)

研究者

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