Clinical Effectiveness Of The Newer Antipsychotic Compounds Olanzapine, Quetiapine And Aripiprazole In Comparison With Low Dose Conventional Antipsychotics (Haloperidol And Flupentixol) In Patients With Schizophrenia
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 发起方
- 入组人数
- 149
- 试验地点
- 18
- 主要终点
- Contentment with treatment: Psychiatrist (CGI)
研究概览
简要总结
This study is designed to compare the efficacy and drug tolerability of two strategies for the treatment of schizophrenia. The two strategies consist of utilizing, on the one hand, a conventional antipsychotic like haloperidol or flupentixol and, on the other hand, a newer antipsychotic compound like olanzapine, quetiapine or aripiprazole in patients with schizophrenia.
详细描述
There is agreement in the psychiatry community that the so-called atypical antipsychotics should be considered first choice in the treatment of schizophrenic disorders. However, the general superiority of these newer antipsychotic drugs over the older conventional drugs could not be clearly demonstrated in recent controlled clinical trials. The discrepancy between every day's clinical perception and the results of clinical trials raises the question whether the studies performed so far employed the adequate methodological approach to represent the daily practice situation which is characterized by a wide variety of duration and type of the schizophrenic disorder, concomitant diseases, and medications. Moreover, some studies might not have been focused adequately on patient-relevant outcome variables.
The present study project is designed to answer these open questions. The innovative character of the study design is
- that different neuroleptic strategies will be compared rather than single antipsychotic drugs, using
- an enhanced biometric design, that provides a choice of treatment with respect to the individual patient though the trial as such is randomised controlled and double blind;
- that clinically relevant endpoints such as quality of life will be the primary variables, and
- inclusion and exclusion criteria lead to a study population representing clinical every day practice as near as possible.
Another innovatory procedure is that serum levels of the study drugs will be recorded twice during the study. The authors hope that their design might yield transfer effects for other clinical trials facing similar problems.
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
- Triple (Participant, Care Provider, Investigator)
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
- 否
入选标准
- •Schizophrenia
- •age 18-65 years
- •necessity to establish new or change antipsychotic treatment due to unsatisfying results or side effects
- •written informed consent
- •Exclusion Criteria (amongst others):
- •Known or suspected hypersensitivity to olanzapine, quetiapine, aripiprazole, flupentixol or haloperidol
- •Acute suicidal tendency
- •"Einwilligungsvorbehalt (BGB)" or "Unterbringung (PsychKG)"
- •Organic psychosis
- •Parkinson Disease
- •History of malignant neuroleptic syndrome
- •QTc interval ≥ 0.5s / history of congenital QTc prolongation
排除标准
- 未提供
研究组 & 干预措施
atypical antipsychotics
Olanzapine, Quetiapine, or Aripiprazole
干预措施: Olanzapine (Drug)
atypical antipsychotics
Olanzapine, Quetiapine, or Aripiprazole
干预措施: Quetiapine (Drug)
typical antipsychotics
Haloperidol or Flupentixol
干预措施: Haloperidol (Drug)
atypical antipsychotics
Olanzapine, Quetiapine, or Aripiprazole
干预措施: Aripiprazole (Drug)
typical antipsychotics
Haloperidol or Flupentixol
干预措施: Flupentixol (Drug)
结局指标
主要结局
Contentment with treatment: Psychiatrist (CGI)
时间窗: 24 weeks
Contentment with treatment: Patient (SF-36)
时间窗: 24 weeks
次要结局
- Subscores of SF-36(24 weeks)
- Subjective wellbeing under neuroleptic treatment scale (SWN-K)(24 weeks)
- Positive and Negative Syndrome Scale (PANSS)(24 weeks)
研究者
Prof. Dr. Eckart Rüther
Principal Investigator
University of Bremen
