Department of Family Medicine, McMaster University, Hamilton, ON, Canada.
Pfizer Vaccine Trial Participant (2020), University of Buenos Aires, Buenos Aires, Argentina.
Int J Risk Saf Med. 2023;34(2):121-128. doi: 10.3233/JRS-220043.
Best practice consent forms in company clinical trials detail the financial coverage for medical treatment of injuries. In trials undertaken for licensing purposes these arrangements can raise concerns. We detail three cases in which elements of the consent forms appear misleading and designed to elicit a consent to participation that might not be forthcoming if volunteers for these clinical trials were aware that what is outlined in principle is not likely to happen in practice. Beyond clinical trial participants, these consent forms have wider implications. Medical coverage of injuries sustained in a clinical trial is a nexus where business, scientific and ethical considerations meet. It is not clear that anyone to date has grappled with the issues posed. This paper uses three clinical trials to illustrate the problems to be addressed.
企业临床试验中的最佳实践知情同意书详细说明了医疗救治损伤的财务覆盖范围。在出于许可目的而进行的试验中,这些安排可能会引起关注。我们详细介绍了三个案例,其中知情同意书的某些内容似乎具有误导性,旨在诱使人们同意参与,如果这些临床试验的志愿者意识到原则上规定的内容在实践中不太可能发生,他们可能不会同意参与。这些知情同意书不仅涉及临床试验参与者,还具有更广泛的影响。临床试验中受伤的医疗保障是商业、科学和伦理考虑因素交汇的地方。目前尚不清楚是否有人已经解决了这些问题。本文使用三个临床试验来说明需要解决的问题。