Informed consent in medical research /
| Other Authors: | , |
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| Format: | Book |
| Language: | English |
| Published: |
London :
BMJ Books,
[2001]
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| Subjects: |
Table of Contents:
- Pt. 1. Informed consent and medical research : a historical perspective
- The Nuremberg Code and the Helsinki Declaration
- A historical introduction to the requirement of obtaining informed consent from research participants
- Human guinea pigs and the ethics of experimentation : the BMJ's correspondent at the Nuremberg medical trial
- Henry K. Beecher and Maurice Pappworth : informed consent in human experimentation and the physicians' response
- Extracts from Pappworth and Beecher
- Learning from unethical research
- Pt. 2. The BMJ debate : informed consent in medical research
- Informed consent : the intracacies
- Evaluation of a stroke family care worker : results of a randomised controlled trial
- Does HIV status influence the outcome of patients admitted to a surgical intensive care unit? A prospective double blind study
- Journals should not publish research to which patients have not given fully informed consent - with three exceptions
- BMJ's present policy (sometimes approving research in which patients have not given fully informed consent) is wholly correct
- Responses to chapters 7-11 : letters to the BMJ
- Other perspectives following the BMJ articles and correspondence
- Pt. 3. Informed consent and the regulation of medical research
- International regulation, informed consent and medical research
- Informed consent, medical research and the competent adult
- Informed consent, medical research with children
- Informed consent, medical research in psychiatry
- Informed consent and surgical research
- Informed consent and genetic research
- Informed consent and HIV : public health versus private lives
- Informed consent and research on assisted conception
- Informed consent for access to medical records for health services research
- Informed consent, medical research, and healthy volunteers
- Pt. 4. The limits of informed consent in medical research : rights, duties, skills
- Informed consent and human rights in medical research
- 'Fully' informed consent, clinical trials, and the boundaries of therapeutic discretion
- Double standards on informed consent to treatment
- Rights and responsibilities of individuals participating in medical research
- Informed consent in medical research : the consumer's view
- The role of effective communication in obtaining informed consent
- Informed consent and medical education
- Pt. 5. Conclusion
- The moral importance of informed consent in medical research : concluding reflections
- Contrmpporary challenges in clinical research : paying lip service to informed consent