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PROTOCOL – Are investigators’ access to trial data and rights to publish restricted and are trial participants informed about this? A comparison of trial protocols and informed consent materials

机译：议定书 - 调查人员访问试验数据和公布限制的权利，并审判参与者是否通知这一点？试用协议和知情同意材料的比较

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Asger Sand Paludan-Müller; Karsten Juhl Jørgensen; Peter C. Gøtzsche;
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年度 2020
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1. Are investigators’ access to trial data and rights to publish restricted and are potential trial participants informed about this? A comparison of trial protocols and informed consent materials [J] . Paludan-Müller Asger S., Ogden Michelle C., Marquardsen Mikkel, BMC Medical Ethics . 2021,第1期

机译：调查人员是否能够获得审判数据和公布限制的权利，并且是潜在的审判参与者了解这一点？试用协议和知情同意材料的比较
2. Access to medications and medical care after participation in HIV clinical trials: a systematic review of trial protocols and informed consent documents. [J] . HIV clinical trials . 2009,第1期

机译：参加HIV临床试验后可获得药物和医疗服务：对试验方案和知情同意书的系统审查。
3. A pilot study of the quality of informed consent materials for Aboriginal participants in clinical trials. [J] . Russell FM, Carapetis JR, Liddle H, Journal of medical ethics . 2005,第8期

机译：对临床试验中原住民参与者知情同意书质量的一项初步研究。
4. e-Informed Consent in Clinical Trials - ethical considerations [C] . DANIEL PURCARU, LAZAR ONISAI, ANCA PURCARU, Recent advances in applied amp; biomedical informatics and computational engineering in systems applications . 2011

机译：临床试验中的电子知情同意书-伦理考虑
5. The influence of acute illness on the informed consent process in clinical trial participants [D] . Evans, Susan. 2003

机译：急性疾病对临床试验参与者明智同意过程的影响
6. Access to Medications and Medical Care After Participation in HIV Clinical Trials: A Systematic Review of Trial Protocols and Informed Consent Documents [O] . Andrea L. Ciaranello, Rochelle P. Walensky, Paul E. Sax, -1

机译：参加HIV临床试验后获得药物和医疗服务：对试验方案和知情同意文件的系统审查
7. An examination of the effects of a patient-designed-and-informed participant information sheet in comparison with a standard, researcher-designed information sheet on recruitment, retention and understanding: Protocol for a study-within-a-trial [O] . Christopher P. Dwyer, Robert A. Joyce, Eimear M. Bane, 2020

机译：审查患者设计和知情的参与者信息表的影响与招聘，保留和理解的标准，研究员设计的信息表比较：用于学习 - 在-A-In-It审判中的议定书

PROTOCOL – Are investigators’ access to trial data and rights to publish restricted and are trial participants informed about this? A comparison of trial protocols and informed consent materials

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