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北美脊髓损伤治疗临床试验网络:目标与进展。

North American Clinical Trials Network for the Treatment of Spinal Cord Injury: goals and progress.

机构信息

Department of Neurosurgery, The Methodist Hospital, Houston, Texas 77030, USA.

出版信息

J Neurosurg Spine. 2012 Sep;17(1 Suppl):6-10. doi: 10.3171/2012.4.AOSPINE1294.

Abstract

The North American Clinical Trials Network (NACTN) for the Treatment of Spinal Cord Injury is a consortium of 10 neurosurgery departments, a data management center, and a pharmacological center. The NACTN was established with the goal of bringing recent molecular and cell-based discoveries in neuroprotection and regeneration from the laboratory into clinical trials that optimize meaningful data outcomes and maximum safety to patients. The requirements of planning and executing clinical trials in spinal cord injury (SCI) and the steps that the NACTN has taken to address these requirements are discussed and illustrated in articles in this issue of the Journal of Neurosurgery: Spine. The progress that the NACTN has made in meeting these goals can be summarized as organizing a network of hospitals capable of enrolling a sufficient number of patients for conducting Phase I and II trials; creating a Data Management Center and a database of the natural history of recovery after SCI (at the time of this writing 485 patients were enrolled in the database); creating a database of the incidence and severity of complications that occur during acute and subacute treatment after SCI; developing a Pharmacological Center capable of performing pharmacokinetic and pharmacodynamic studies of therapeutic drugs; completing enrollment of 36 patients in NACTN's first clinical trial, a Phase I study of riluzole, a neuroprotective drug; and performing pharmacokinetic and pharmacodynamic studies of riluzole in acute SCI.

摘要

北美脊髓损伤治疗临床试验网络(NACTN)是一个由 10 个神经外科部门、一个数据管理中心和一个药理学中心组成的联盟。该网络的建立目标是将神经保护和再生方面的最新分子和细胞基础研究成果从实验室转化为临床试验,以优化有意义的数据结果并确保患者的最大安全性。本文讨论并说明了规划和执行脊髓损伤(SCI)临床试验的要求,以及 NACTN 为满足这些要求而采取的步骤。NACTN 在实现这些目标方面的进展可以概括为:组织了一个能够招募足够数量的患者进行 I 期和 II 期试验的医院网络;创建了一个数据管理中心和一个 SCI 后自然恢复史数据库(截至本文撰写时,已有 485 名患者入组数据库);创建了一个数据库,记录 SCI 后急性和亚急性治疗期间发生的并发症的发生率和严重程度;开发了一个药理学中心,能够进行治疗药物的药代动力学和药效学研究;完成了 NACTN 首个临床试验的 36 名患者入组,该试验是一种神经保护药物利鲁唑的 I 期研究;并在急性 SCI 中进行了利鲁唑的药代动力学和药效学研究。

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