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- W2058706731 abstract "A British physician outlines six rights of patients that protect their status as equal partners with experimenters in clinical research, the right to know their rights; to understand the experiment (its purpose, how it could affect the patient, and alternative approaches); to refuse information about a bad prognosis; to withdraw from the study at any time; to confidentiality; and to receive a final copy of the report of the study with a summary in nontechnical language. Differing policies on information and consent introduce discrepancies in the selection of subjects between medical centers that may affect the results of a study. Herxheimer recommends that ethics committees include at least two lay members from the community; he sees them as having a crucial role in safeguarding patients' rights and in working toward the establishment of a uniform understanding of these rights among patients and clinicians." @default.
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- W2058706731 date "1988-11-01" @default.
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- W2058706731 title "THE RIGHTS OF THE PATIENT IN CLINICAL RESEARCH" @default.
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- W2058706731 doi "https://doi.org/10.1016/s0140-6736(88)90536-3" @default.
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