药物Ⅰ期临床试验受试者管理方法的探讨

    The Discussion of Volunteer Management Methods in PhaseⅠ Clinical Trials for New Drugs

    • 摘要: 目的 分析Ⅰ期临床试验中影响受试者管理的主要因素,探讨增强受试者依从性、提高试验质量的方法。 方法 比较2008-2011年措施前与2012年措施后受试者招募、知情同意、筛查、试验过程控制和试验后管理情况。 结果 联合使用多种招募方式能增加受试者招募人数,招募时长缩短1倍,为后续的筛查工作提供足够的研究对象。充分的知情、严格的筛查和试验过程培训能增强受试者的依从性;专业的随访有助于受试者评价我们的工作。 结论 通过在受试者招募、知情同意、筛查、试验过程和试验后的受试者管理等环节采取措施能明显增强受试者的依从性,提高试验质量。

       

      Abstract: Objective To analyze the main factors affecting volunteer management in phase I clinical trials and explore the Methods of enhancing the volunteer compliance and the quality of clinical trials. Methods In terms of the volunteer recruitment, informed consent, screening, the control of the trial procedure and the follow-up, we compared the volunteer management before the measures in 2008-2011 and after the measures in 2012. Results The rate of recruited subjects increased and the recruitment period was shortened one fold by the combined recruitment methods. A fully informed consent, strict screening and volunteer training in the trials improved the compliance of the subjects. The professional follow-up was useful for our work. Conclusion Taking effective measures in volunteer management improved the compliance of the subjects, which enhanced the quality of clinical trials.

       

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