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急性精神分裂症研究中的关键试验相关标准。

Critical trial-related criteria in acute schizophrenia studies.

机构信息

Department of Psychiatry and Psychotherapy, Ludwig-Maximilians-University Munich, Nussbaumstrasse 7, 80336, Munich, München, Germany.

出版信息

Eur Arch Psychiatry Clin Neurosci. 2012 Mar;262(2):151-5. doi: 10.1007/s00406-011-0225-3. Epub 2011 Jul 26.

Abstract

The Trial Criteria in Schizophrenia Working Group was convened in November 2007 to define consensus criteria for clinical trials in patients suffering from acute schizophrenia with special focus on placebo-controlled trials and withdrawal conditions. Clinical trials involving patients give rise to ethical and medico-legal dilemmas. Essential research of new drugs may potentially expose patients to ineffective treatment regimens or placebo. The complexity of the problem increases when dealing with mentally ill patients. The Working Group's criteria are thought to cover different aspects important in conducting clinical trials namely to ensure the patient's safety, to present criteria that would allow the ethics committees to agree to the proposed criteria and to enable the possibility to reasonably conduct and ensure comparable quality of clinical studies in acutely ill patients with schizophrenia. To furthermore counteract current inconsistencies, these criteria should be evaluated using standardized rating scales applying established cut-off criteria. The developed trial criteria cover inclusion and exclusion criteria as well as withdrawal criteria due to non-response or worsening of symptoms.

摘要

精神分裂症临床试验标准工作组于 2007 年 11 月成立,旨在为急性精神分裂症患者的临床试验(尤其关注安慰剂对照试验和退出条件)制定共识标准。涉及患者的临床试验引发了伦理和医疗法律方面的困境。新药的基本研究可能会使患者面临无效的治疗方案或安慰剂。当涉及精神疾病患者时,问题的复杂性会增加。工作组的标准被认为涵盖了进行临床试验的重要方面,包括确保患者的安全,提出符合伦理委员会要求的标准,并使合理开展并确保患有急性精神分裂症的患者的临床研究具有可比性质量成为可能。为了进一步消除当前的不一致性,这些标准应使用应用既定截止标准的标准化评分量表进行评估。制定的临床试验标准涵盖了纳入和排除标准以及因无反应或症状恶化而退出的标准。

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