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Oxford textbook of clinical research ethics

https://bccalibrary.andornot.com/en/permalink/catalog17845
New York, NY: Oxford University Press , 2008.
Audience
Professional
Call Number
W20.55 H9 O98 2008
Availability
5 copies, 5 available
I: Selected history of research with humans; Walter Reed and the yellow fever experiments by Susan E. Lederer; Nazi medical experiments by Paul J. Weindling; Imperial Japanese experiments in China by Takashi Tsuchiya; Randomized controlled trial of streptomycin by Alan Yoshioka; Salk polio vaccine …
Editor
Emanuel, Ezekiel J
Place of Publication
New York, NY
Publisher
Oxford University Press
Publication Date
2008
Physical Description
xx, 827 p. : ill. ; 29 cm.
Subjects
Human Experimentation - ethics
Ethics, Research
Ethics Committees, Research
Research Subjects - legislation & jurisprudence
Abstract
I: Selected history of research with humans
Walter Reed and the yellow fever experiments by Susan E. Lederer
Nazi medical experiments by Paul J. Weindling
Imperial Japanese experiments in China by Takashi Tsuchiya
Randomized controlled trial of streptomycin by Alan Yoshioka
Salk polio vaccine field trial of 1954 by Marcia L. Meldrum
Jewish chronic disease hospital case by John D. Arras
Hepatitis experiments at the Willowbrook State School by Walter M. Robinson and Brandon T. Unruh
Tuskegee syphilis experiment by James H. Jones
HIV research by John Y. Killen Jr.
Gelsinger case by Robert Steinbrook II: Codes, declarations, and other ethical guidance for research with humans
Ethical framework for biomedical research by Ezekiel J. Emanuel, David Wendler and Christine Grady
Nuremberg code by George J. Annas and Michael A. Grodin
Declaration of Helsinki by Richard E. Ashcroft
Belmont report by Tom L. Beauchamp
Regulations for the protection of humans in research in the United States: The common rule by Joan P. Porter and Greg Koski
International ethical guidance rrom the Council for International Organizations of Medical Sciences by Juhana E. ldanpaan-Heikkila and Sev S. Fluss
Council of Europe by Peteris Zilgalvis
European Community directives on data protection and clinical trials by Deryck Beyleveld and Sebastian Sethe
National bioethics commissions and research ethics by Eric M. Meslin and Summer Johnson III. Context, purpose, and value of clinical research
Exploitation in clinical research by Alan Wertheimer
Nature, scope, and justification of Clinical Research : what Is research? Who Is a subject? by Robert J. Levine
Four paradigms of clinical research and research oversight by Ezekiel J. Emanuel and Christine Grady
Role of patient advocates and public representatives in research by Rebecca Dresser IV. Scientific design
Equipoise and randomization by Steven Joffe and Robert D. Truog
Ethics of placebo-controlled trials by Franklin G. Miller
Challenge experiments by Franklin G. Miller and Donald L. Rosenstein
Emergency research by Jason H. T. Karlawish
Research with biological samples by David Wendler
Genetic diagnostic, pedigree, and screening research by Eric T. Juengst and Aaron Goldenberg
Deception in clinical research by David Wendler and Franklin G. Miller
Epidemiology : observational studies on human populations by Douglas L. Weed and Robert E. McKeown
Behavioral and social science research by Felice J. Levine and Paula R. Skedsvold
Phase I Oncology research by Manish Agrawal and Ezekiel J. Emanuel
Surgical innovation and research by Grant R. Gillett V. Participant selection Sect. A. Fair Participant selection
What Is fair participant selection? by Leslie A. Meltzer and James F. Childress
Incentives for research participants by Neal Dickert and Christine Grady
Recruiting research participants by Franklin G. Miller
Sect. B. Special populations
Research involving women by Christine Grady and Colleen Denny
Research with ethnic and minority populations by Bernard Lo and Nesrin Garan
Research involving economically disadvantaged participants by Carol Levine
Research involving those at risk for impaired decision-making capacity by Donald L. Rosenstein and Franklin G. Miller
Research with children by Alan R. Fleischman and Lauren K. Collogan
Research with captive populations :prisoners, students, and soldiers by Valerie H. Bonham and Jonathan D. Moreno
Research with identifiable and targeted communities by Morris W. Foster and Richard R. Sharp
Research with healthy volunteers by Albert R. Jensen and Franklin G. Miller
Research with fetuses, embryos, and stem cells by Ronald M. Green VI. Risk-benefit assessments
Risk-benefit analysis and the net risks test by David Wendler and Franklin G. Miller
Assessing and comparing potential benefits and risks of harm by Nancy M. P. King and Larry R. Churchill
Risk-benefit assessment in pediatric research by Sumeeta Varma and David Wendler VII. Independent review and oversight
Origins and policies that govern institutional review boards by Charles R. McCarthy
Models of institutional review board function by Angela J. Bowen
Evaluating the effectiveness of institutional review boards by Marjorie A. Speers
Data and safety monitoring boards by Lawrence M. Friedman and Eleanor B. Schron
Food and drug administration and drug development : historic, scientific, and ethical considerations by Robert Temple and Sara F. Goldkind VIII. Informed consent
History of informed consent in clinical research by Erika Blacksher and Jonathan D. Moreno
Philosophical justifications of informed consent in research by Dan W. Brock
Legal and regulatory standards of informed consent in research by Alexander M. Capron
Therapeutic misconception by Paul S. Appelbaum and Charles W. Lidz
Empirical issues in informed consent for research by James H. Flory, David Wendler and Ezekiel J. Emanuel
Assent requirement in pediatric research by David Wendler IX. Respect for human research participants
Confidentiality by James G. Hodge Jr. and Lawrence O. Gostin
Liability and compensation for injury of research subjects by Wendy K. Mariner
Obligation to ensure access to beneficial treatments for research participants at the conclusion of clinical trials by James V. Lavery X. Multinational research
Appropriate ethical standards by Ruth Macklin
Benefits to host countries by Ezekiel J. Emanuel
Standard of care in multinational research by Soren Holm and John Harris
Responsiveness to host community health needs by Alex John London XI. Clinical investigator behavior
Conflict of interest in medical research : historical developments by Trudo Lemmens
Concept of conflicts of interest by Ezekiel J. Emanuel and Dennis F. Thompson
Empirical data on donflicts of interest by Lindsay A. Hampson, Justin E. Bekelman and Cary P. Gross
Industrialization of academic science and threats to scientific integrity by Eric G. Campbell and David Blumenthal
Fraud, fabrication, and falsification by David B. Resnik
Obligation to publish and disseminate results by Drummond Rennie.
ISBN
9780195168655
0195168658
Language
English
Material Type
Book
Audience
Professional
Location
Vancouver Library
Kelowna Library
Surrey Library
Victoria Library
Abbotsford Library
Call Number
W20.55 H9 O98 2008

Copies

c.1 BC Cancer Agency ARHCC Library Available
c.1 BC Cancer Agency KEL Library Available
c.1 BC Cancer Agency SUR Library Available
c.1 BC Cancer Agency VAN Library Available
c.1 BC Cancer Agency VIC Library Missing Available
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