Informed consent in medical research.doi:10.1054/bjoc.2001.2135DRnzoBritish Journal of Cancer
Informed consent in medical research2001 Cancer Research Campaigndoi:10.1054/bjoc.2001.2135E G DeRenzoBritish Journal of Cancer
This is a comprehensive discussion of the ethical issues involved in informing patients on their rights and participation in medical research and treatment. With 30 chapters contributed by internationally recognised medical ethicists, Informed Consent provides an authoritative reference on a subject of major...
摘要: Argues that the principle of informed consent in medical research is fundamental if patients are competent volunteers. Conditions for and exemptions from requiring informed consent; Conditions for publishing medical researches; Recommended policies for medical journals....
医学英语文献阅读informed consent Informed consent is an integral part of healthcare and medical research, ensuring that patients and participants have a clear understanding of the procedures, risks, and benefits involved in their treatment or study participation. It is a fundamental ethical principle ...
Informed consent in medical research. 来自 NCBI 喜欢 0 阅读量: 34 作者: L Doyal,JS Tobias,M Warnock,L Power,H Goodare 展开 摘要: The BJC is owned by Cancer Research UK, a charity dedicated to understanding the causes, prevention and treatment of cancer and to making sure that ...
2.1. Informed Consent in Medical Care As mentioned prior, the main focus of this manuscript is discussing informed consent in biomedical research. While not immediately related to research-at-hand, informed consent in medical practice is still a vital subset of the evolution of the modern form of...
The consent document must state (ICH GCP 4.8.10): The anticipated prorated payment, if any, to the participant for participating in the trial. Points to note: Payment to participants for their participation in a research study must never be coercive in either amount or method of distribution...
There are 4 principles of informed consent: You must have the capacity (or ability) to make the decision. The medical provider must disclose information on the treatment, test, or procedure in question, including the expected benefits and risks, and the likelihood (or probability) that the bene...
informed consentAcute myocardial infarction (AMI) is a common disease in the Western world and has been the topic of much research. Conducting clinical trials with patients in the acute phase of a myocardial infarction, however, poses an ethical challenge. As patients are often under extreme ...