dc.creator | Daugherty, Christopher K. | en |
dc.creator | Siegler, Mark | en |
dc.creator | Ratain, Mark J. | en |
dc.creator | Zimmer, George | en |
dc.date.accessioned | 2015-05-05T18:59:19Z | en |
dc.date.available | 2015-05-05T18:59:19Z | en |
dc.date.created | 1997-06-01 | en |
dc.date.issued | 1997-06-01 | en |
dc.identifier | 10.7326/0003-4819-126-11-199706010-00008 | en |
dc.identifier.bibliographicCitation | Annals of Internal Medicine. 1997 Jun 1; 126(11): 892-897. | en |
dc.identifier.issn | 0003-4819 | en |
dc.identifier.uri | http://worldcatlibraries.org/registry/gateway?version=1.0&url_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&atitle=Learning+from+Our+Patients:+One+Participant's+Impact+on+Clinical+trial+Research+and+Informed+Consent&title=Annals+of+Internal+Medicine.++&volume=126&issue=11&pages=892-897&date=1997&au=Daugherty,+Christopher+K. | en |
dc.identifier.uri | http://dx.doi.org/10.7326/0003-4819-126-11-199706010-00008 | en |
dc.identifier.uri | http://hdl.handle.net/10822/750771 | en |
dc.description.abstract | This Perspective includes an essay on modifying phase I clinical
trials, written by George Zimmer, who was a professor of English and a
commentary on that essay. Professor Zimmer was a cancer patient who
participated in the phase I clinical trial program at the University of
Chicago. His ideas are eloquently expressed and have had a profound effect on
our investigational research for anticancer agents. Although at times his
suggestions may seem radical, Professor Zimmer urges us to reconsider the
50-year-old Nuremberg paradigm that participants in human research are
ignorant and vulnerable and must be protected. Although we must protect
patients who have life-threatening diseases from coercive inducements and
misplaced hopes, we must also listen carefully and thoughtfully to our
patients. This is particularly true when, as research participants in the face
of sacrifice and the threat of a life-ending diagnosis, they have made the
effort to express their concerns. With the effect of the acquired
immunodeficiency syndrome movement on clinical studies and on drug research
and development, a precedent has been set that allows patients to reshape
their role as participants in research trials. On a personal level, the essay
by Professor Zimmer has had a significant effect on our research methods and,
indeed, the focus of our research efforts. Thus, it is with a sense of respect
and honor that we share George Zimmer's thoughts and our comments about the
influence he has had on our research practices. | en |
dc.format | Article | en |
dc.language | en | en |
dc.source | BRL:MEDKIE/97298581 | en |
dc.subject | Aids | en |
dc.subject | Attitudes | en |
dc.subject | Autonomy | en |
dc.subject | Acquired Immunodeficiency Syndrome | en |
dc.subject | Cancer | en |
dc.subject | Clinical Trials | en |
dc.subject | Comprehension | en |
dc.subject | Control Groups | en |
dc.subject | Consent | en |
dc.subject | Decision Making | en |
dc.subject | Diagnosis | en |
dc.subject | Drugs | en |
dc.subject | Empirical Research | en |
dc.subject | Federal Government | en |
dc.subject | Food | en |
dc.subject | Government | en |
dc.subject | Human Experimentation | en |
dc.subject | Informed Consent | en |
dc.subject | Investigators | en |
dc.subject | Life | en |
dc.subject | Methods | en |
dc.subject | Motivation | en |
dc.subject | Paternalism | en |
dc.subject | Patient Advocacy | en |
dc.subject | Patient Participation | en |
dc.subject | Patients | en |
dc.subject | Political Activity | en |
dc.subject | Regulation | en |
dc.subject | Research | en |
dc.subject | Research Design | en |
dc.subject | Research Subjects | en |
dc.subject | Risks and Benefits | en |
dc.subject | Terminally Ill | en |
dc.subject | Vulnerable Populations | en |
dc.title | Learning From Our Patients: One Participant's Impact on Clinical Trial Research and Informed Consent | en |
dc.provenance | Digital citation created by the National Reference Center for Bioethics Literature at Georgetown University for the BIOETHICSLINE database, part of the Kennedy Institute of Ethics' Bioethics Information Retrieval Project funded by the United States National Library of Medicine. | en |
dc.provenance | Digital citation migrated from OpenText LiveLink Discovery Server database named NBIO hosted by the Bioethics Research Library to the DSpace collection BioethicsLine hosted by Georgetown University. | en |