In this study,we are discussing the rationale behind informed consent in clinical trials in developing countries.It elaborates how informed consent has remained an ethical and practical issue.Poverty,endemic diseases,and a lack of investment in healthcare systems influence the ease of conducting and ...
INFORMED CONSENT IN CLINICAL TRIALS FOR PERSONS WITH DEMENTIA Informed consent is one of the most important processes during the implementation of a clinical trial; special attention must be given to meeting the needs of persons with dementia in nursing homes who have impaired decision making capac...
This study demonstrates difficulties experienced in obtaining consent from critically ill patients to participate in medical research and raises important issues about the ethical basis of the consent process in critical care. 展开 关键词: Intensive care Clinical trial Ethics Consent ...
Informed Consent for Clinical Trials for People with Disabilities Complement your general informed consent form with this template, which can be used with clinical trial subjects with disabilities. Use this form when enrolling subjects with physical challenges (e.g., subjects unable to speak or write...
Paternalism has slowly gone the way of the long-play record, and in its place has emerged a consent process in which the patient is a more fully informed and active participant. This process takes time however, and for the busy health-care provider there is often the temptation to hand ...
To compare the informed consent processes for phase III pediatric and adult oncology clinical trials in view of the critical importance of human subjects protection in both pediatric and adult cancer care. Findings are discussed in terms of the opportunities for improving pediatric and adult oncology ...
Informed consent in clinical trials. Consent may not be possible P Chinnery,George_Asimakopoulos,R Kenny - 《Bmj Clinical Research》 被引量: 0发表: 1994年 Genetic and neurochemical modulation of prefrontal cognitive functions in children. The catechol O-methyltransferase (COMT) gene affects how ...
PURPOSE/: To review the issues related to informed consent in a clinical care setting and suggest strategies to improve the informed consent process.: Published books, journal articles, and clinical research experience.: Clinicians and researchers are ethically obligated to maintain the informed consent...
Ⅰ、Informed consent is a process by which a person voluntarily agrees to participate in a research study after being fully informed about it. 1、知情同意是指 一个人在完全知情后自愿同意参与研究的过程 。 Ⅱ、The informed consent document should contain all of the information that the particip...
The consent process must also include a full description of alternative strategies that might be employed in a similar clinical setting. Again, investigators must include an objectively valid description of the known risks and benefits of these alternative approaches. This is the case whether the alte...