The Oxford textbook of clinical research ethics

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The Oxford textbook of clinical research ethics / edited by Ezekiel J. Emanuel ... [et al.]

資料種別:

図書

出版情報:

New York, N.Y. : Oxford University Press, 2010

形態:

xx, 827 p. ; 28 cm

著者名:

Emanuel, Ezekiel J., 1957- <DA06063182>

Grady, Christine <DA09860449>

Crouch, Robert A.

Lie, Reidar K. <DA14053107>

Miller, Franklin G. <DA16996553>

Wendler, David <DA1763643X>

さらに 1 件

ISBN:

9780199768639 [0199768633] (: pbk)

書誌ID:

BB10579634

子書誌情報

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所蔵情報

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書誌詳細

その他の標題:

Textbook of clinical research ethics

注記:

Other editors: Christine Grady, Robert A. Crouch, Reidar K. Lie, Franklin G. Miller, David Wendler
Includes bibliographical references and index

主題:

Clinical trials--Moral and ethical aspects; Human experimentation in medicine--Moral and ethical aspects; Medical ethics

言語:

英語

目次情報:

The History of Research with Humans / Part 1：

Walter Reed and the Yellow Fever Experiments / 1：

The Nazi Medical Experiments / 2：

The Imperial Japanese Experiments in China / 3：

The Randomized Controlled Trial of Streptomycin / 4：

The Salk Polio Vaccine Field Trial of 1954 / 5：

The Jewish Chronic Disease Hospital Case / 6：

The Hepatitis Experiments at the Willowbrook State School / 7：

The Tuskegee Syphilis Experiment / 8：

HIV Research / 9：

The Gelsinger Case / 10：

An Ethical Framework for Biomedical Research / 11：

Codes, Declarations, and Other Ethical Guidance for Research with Humans / Part 2：

The Nuremberg Code / 12：

The Declaration of Helsinki / 13：

The Belmont Report / 14：

Regulations for the Protection / 15：

International Ethical Guidance from the Council for International Organizations of Medical Sciences / 16：

The Council of Europe / 17：

The European Community Directives on Data Protection and Clinical Trials / 18：

National Bioethics Commissions and Research / 19：

Context, Purpose, and Value of Clinical Research / Part 3：

Exploitation in Clinical Research / 20：

The Nature, Scope, and Justification of Clinical research: What is Research? Who is a Subject? / 21：

Four Paradigms of Clinical Research and Research Oversight / 22：

The Role of Patient Advocates and Public Representatives in Research / 23：

Scientific Design / Part 4：

Equipoise and Randomization / 24：

The Ethics of Placebo- Controlled Trials / 25：

Challenge Experiments / 26：

Emergency Research / 27：

Consent for Research with Biological Samples / 28：

Genetic Diagnostic, Pedigree, and Screening Research / 29：

Deception in Clinical Research / 30：

Ethics of Epidemiology: Observational Studies on Human Populations / 31：

Ethical Issues in Behavioral and Social Science Research / 32：

Phase 1 Oncology Research / 33：

Surgical Innovation and Research / 34：

Participant Selection / Part 5：

What is Fair in Participant Selection? / 35：

Incentives for Research Participants / 36：

Ethical Issues in Recruiting Research Participants / 37：

Ethical Issues in Research Involving Women / 38：

Ethical Issues in Research with Ethnic and Minority Populations / 39：

Research Involving Economically Disadvantaged Participants / 40：

Research Involving Those at Risk for Impaired Decision-making Capacity / 41：

Research with Children / 42：

Captive Populations: Prisoners, Students, and Soldiers / 43：

Research with Identifiable and Targeted Communities / 44：

Research with Health Volunteers / 45：

Research with Fetuses, Embryos, and Stem Cells / 46：

Risk-Benefit Assessments / Part 6：

Risk-Benefit Analysis and the Net Risks Test / 47：

Assessing the Comparing Potential Benefits and Risks of Harm / 48：

Risk-Benefit Assessment in Pediatric Research / 49：

Independent Review and Oversight / Part 7：

Institutional Review Boards: Their Origins and the Policies that Govern Them / 50：

Models of Institutional Review Board Function / 51：

Assessing and Comparing Potential Benefits and Risks of Harm / 52：

Data and Safety Monitoring Boards / 53：

The Food and drug Administration and Drug Development: Historic, Scientific, and Ethical Considerations / 54：

Informed Consent / Part 8：

A History of Informed Consent in Clinical Research / 55：

Philosophical Justifications of Informed Consent in Research / 56：

Legal and Regulatory Standards of Informed Consent in Research / 57：

The Therapeutic Misconception / 58：

Empirical Issues in Informed Consent for Research / 59：

The Assent Requirement in Pediatric Research / 60：

Respect for Human Research Participants / Part 9：

Confidentiality / 61：

Legal Responsibility to Research Subjects: Liability and Compensation for Injury / 62：

The Obligation to Ensure Standards / 63：

Multi-National Research / Part 10：

Appropriate Standards / 64：

Benefits to Host Countries / 65：

The Standard of Care in Multi-National Research / 66：

Responsiveness to Host Community Health Needs / 67：

Clinical Investigator Behavior / Part 11：

Conflicts of Interest in Medical Research: historical Developments / 68：

Conflicts of Interest / 69：

Empirical Data on Obligations of Publication: Authorship and Dissemination / 70：

Index

The History of Research with Humans / Part 1：

Walter Reed and the Yellow Fever Experiments / 1：

The Nazi Medical Experiments / 2：

The Imperial Japanese Experiments in China / 3：

The Randomized Controlled Trial of Streptomycin / 4：

The Salk Polio Vaccine Field Trial of 1954 / 5：

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