The Oxford textbook of clinical research ethics

(ed.)
New York: Oxford University Press (2008)
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Abstract

Comprehensive in scope and research, this book will be a crucial resource for researchers in the medical sciences, as well as teachers and students alike.

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R853.H8.O96 2008

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9780195168655   0195168658

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Chapters

Conflicts of Interest.Dennis F. Thompson & E. Emmanuel
Equipoise and Randomization.Steven Joffe Robert D. Truog
Four Paradigms of Clinical Research and Research Oversight.Ezekiel J. Emanuel Christine Grady
HIV research.John Y. Killen Jr
National Bioethics Commissions and Research Ethics.Eric M. Meslin Summer Johnson
Philosophical justifications of informed consent in research.D. Brock, E. J. Emanuel, C. Grady, R. Lie, F. Miller & D. Wendler
What Is Fair Participant Selection?Leslie Meltzer Henry & James Childress
Research with ethnic and minority populations.  (pages 1--423)Bernard Lo & N. Garan
Ezekiel J. Emanuel.  (pages 3)Reidar K. Lie
Research With Identifiable and Targeted Communities.  (pages 6--475)Morris W. Foster
Walter Reed and the yellow fever experiments.  (pages 9--17)Susan E. Lederer
The Nazi Medical Experiments.  (pages 18)Paul J. Weindling
The imperial Japanese experiments in China.  (pages 31)Takashi Tsuchiya
The Randomized Controlled Trial of Streptomycin.  (pages 46)Alan Yoshioka
The Salk Polio Vaccine Field Trial of 1954.  (pages 61)Marcia L. Meldrum
The Jewish chronic disease hospital case.  (pages 73)John D. Arras
The Hepatitis Experiments at the Willowbrook State School.  (pages 80)Walter M. Robinson Brandon T. Unruh
The Gelsinger case.  (pages 110)Robert Steinbrook
An ethical framework for biomedical research.  (pages 123--135)Ezekiel J. Emanuel, David Wendler & C. Grady
The declaration of Helsinki.  (pages 141--148)Richard Ashcroft
The Belmont Report.  (pages 149--55)Tom L. Beauchamp
Regulations for the Protection of Humans in Research in the United States.  (pages 156)Joan P. Porter & Greg Koski
The Council of Europe.  (pages 174)Pēteris Zilgalvis
The European Community Directives on Data Protection and Clinical Trials.  (pages 180)Deryck Beyleveld Sebastian Sethe
National bioethics commissions and research ethics.  (pages 187)E. Meslin & Summer Johnson
Exploitation in clinical research.  (pages 201--10)Alan Wertheimer
The Nature, Scope, and Justification of Clinical Research.  (pages 211)Robert J. Levine
The role of patient advocates and public representatives in research.  (pages 231)Rebecca Dresser
Equipoise and randomization.  (pages 245--60)Steven Joffe & R. Truog
The ethics of placebo-controlled trials.  (pages 261)Franklin G. Miller
The Nuremberg Code.  (pages 266-266)George J. Annas Michael A. Grodin
Challenge Experiments.  (pages 273)Franklin G. Miller & D. L. Rosenstein
Emergency research.  (pages 280)J. H. Karlawish
Research with biological samples.  (pages 290--297)David Wendler
Genetic diagnostic, pedigree, and screening research.  (pages 298)Eric T. Juengst & Aaron Goldenberg
Observational Studies on Human Populations.  (pages 325)Douglas L. Weed & Robert E. McKeown
Behavioral and Social Science Research.  (pages 336)Felice J. Levine & Paula R. Skedsvold
Phase I Oncology Research.  (pages 356)Manish Agrawal
Surgical Innovation and Research.  (pages 367)Grant R. Gillett
Incentives for Research Participants.  (pages 386)Neal Dickert & Christine Grady
Recruiting Research Participants.  (pages 397)Franklin G. Miller
Research Involving Women.  (pages 407)Colleen Denny
Research Involving Economically Disadvantaged Participants.  (pages 431)Carol Levine
Research involving those at risk for impaired decision-making capacity.  (pages 437--445)Donald L. Rosenstein & Franklin G. Miller
Research with captive populations.  (pages 461--474)Valerie H. Bonham & Jonathan D. Moreno
Legal and regulatory standards of informed consent in research.  (pages 613--32)A. M. Capron
The therapeutic misconception.  (pages 633--644)P. S. Applebaum & C. Lidz
Empirical issues in informed consent for research.  (pages 645--60)James Flory, David Wendler & Ezekiel Emanuel
The assent requirement in pediatric research.  (pages 661--671)D. Wendler
The obligation to ensure access to beneficial treatments for research participants at the conclusion of clinical trials.  (pages 697--710)J. V. Lavery
Conflict of interest in medical research. Historical developments.  (pages 747--757)T. Lemmens
The concept of conflicts of interest.  (pages 758--766)Ezekiel J. Emanuel & Dennis F. Thompson
Empirical data on conflicts of interest.  (pages 767--779)L. A. Hampson, J. E. Bekelman & C. P. Gross
Fraud, fabrication, and falsification.  (pages 787--794)D. Resnik

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Citations of this work

An Ethical Framework for Evaluating Experimental Technology.Ibo van de Poel - 2016 - Science and Engineering Ethics 22 (3):667-686.
Rethinking the Belmont Report?Phoebe Friesen, Lisa Kearns, Barbara Redman & Arthur L. Caplan - 2017 - American Journal of Bioethics 17 (7):15-21.

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