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The ethical analysis of risk in intensive care unit researchHelsinki discords: FDA, ethics, and international drug trialsRisk, diagnostic error, and the clinical science of consciousnessEthics of neuroimaging after serious brain injury.Ethics, economics and the regulation and adoption of new medical devices: case studies in pelvic floor surgery.How to design efficient cluster randomised trials.Ethics. Protecting communities in biomedical research.The publication of ethically uncertain research: attitudes and practices of journal editorsThe Ottawa Statement on the Ethical Design and Conduct of Cluster Randomized Trials.Requirements for ethics committee review for studies submitted to Implementation ScienceInadequate reporting of research ethics review and informed consent in cluster randomised trials: review of random sample of published trials.Ethical issues posed by cluster randomized trials in health research.Does clinical equipoise apply to cluster randomized trials in health research?Disclosure of the right of research participants to receive research results: an analysis of consent forms in the Children's Oncology Group.Who is the research subject in cluster randomized trials in health research?When is informed consent required in cluster randomized trials in health research?A Scoping Review of Empirical Research Relating to Quality and Effectiveness of Research Ethics Review.Mail merge can be used to create personalized questionnaires in complex surveys.Acknowledging awareness: informing families of individual research results for patients in the vegetative state.Protocol for the development of a CONSORT-equity guideline to improve reporting of health equity in randomized trials.What is the role and authority of gatekeepers in cluster randomized trials in health research?The ethics of future trials: qualitative analysis of physicians' decision makingResearchers' perceptions of ethical challenges in cluster randomized trials: a qualitative analysis.Trust based obligations of the state and physician-researchers to patient-subjects.Accumulating Evidence and Research Organization (AERO) model: a new tool for representing, analyzing, and planning a translational research program.Ethics of surgical training in developing countries.U.S. Federal Regulations for emergency research: a practical guide and commentary.Providing research results to participants: attitudes and needs of adolescents and parents of children with cancer.Ethical issues associated with the introduction of new surgical devices, or just because we can, doesn't mean we should.Ethical and policy issues in cluster randomized trials: rationale and design of a mixed methods research study.A comparison of journal instructions regarding institutional review board approval and conflict-of-interest disclosure between 1995 and 2005.Covert narrative capacity: Mental life in patients thought to lack consciousness.Variability in research ethics review of cluster randomized trials: a scenario-based survey in three countries.Considerations and costs of disclosing study findings to research participants.Impact of CONSORT extension for cluster randomised trials on quality of reporting and study methodology: review of random sample of 300 trials, 2000-8.Reporting of patient consent in healthcare cluster randomised trials is associated with the type of study interventions and publication characteristics.Challenges in the research ethics review of cluster randomized trials: international survey of investigators.Position statement on ethics, equipoise and research on charged particle radiation therapy.Cluster-randomized trials: A closer look.What questions can a placebo answer?
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P50
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Charles Weijer
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Charles Weijer
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Charles Weijer
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Charles Weijer
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Charles Weijer
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Charles Weijer
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Charles Weijer
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Charles Weijer
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Charles Weijer
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Charles Weijer
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Charles Weijer
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Charles Weijer
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P31
P496
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