Research Topics
| C WeijerSummaryAffiliation: Dalhousie University Country: Canada Publications
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Detail Information
Publications
When are research risks reasonable in relation to anticipated benefits?Charles Weijer
Department of Bioethics, Dalhousie University, 5849 University Avenue, Halifax, Nova Scotia B3H 4H7, Canada
Nat Med 10:570-3. 2004
The ethics of placebo-controlled trialsCharles Weijer
Department of Bioethics, Dalhousie University, Halifax, Nova Scotia, Canada
J Bone Miner Res 18:1150-3. 2003
Continuing review of clinical research Canadian-styleCharles Weijer
Department of Bioethics, Dalhousie University, Halifax, NS
Clin Invest Med 25:92-3. 2002
A death in the family: reflections on the Terri Schiavo caseCharles Weijer
McMaster University, Hamilton, Ont
CMAJ 172:1197-8. 2005
Refuting the net risks test: a response to Wendler and Miller's "Assessing research risks systematically"C Weijer
Department of Philosophy, Talbot College, University of Western Ontario, London, Ontario, Canada, N6A 3K7
J Med Ethics 33:487-90. 2007..This response argues that the net risks test meets none of these criteria and concludes that it is not a viable alternative to component analysis...
Protecting communities in pharmacogenetic and pharmacogenomic researchC Weijer
Department of Bioethics, Dalhousie University, Halifax, Nova Scotia, Canada
Pharmacogenomics J 4:9-16. 2004..Rather, application of these policy protections must take into account particulars of both planned research and the communities involved...
The ethical analysis of risk in intensive care unit researchCharles Weijer
Dalhousie University, Halifax, Canada
Crit Care 8:85-6. 2004..This realization has important implications for review by institutional review boards of such research and for the informed consent process...
The quest for legitimacy: comment on Cox Macpherson's 'To strengthen consensus, consult the stakeholders'Charles Weijer
Deparment of Bioethics, Dalhousie University, 5849 University Avenue, Halifax, Nova Scotia, Canada, B3H 4H7
Bioethics 18:293-300. 2004
Ethics. Protecting communities in biomedical researchC Weijer
Department of Bioethics, Dalhousie University, Halifax, Nova Scotia, B3H 4H7, Canada
Science 289:1142-4. 2000..Depending on the particular community, consent and consultation, consultation alone, or no added protections may be required for research...
Protecting communities in research: current guidelines and limits of extrapolationC Weijer
Department of Bioethics, Dalhousie University, Halifax, Nova Scotia, Canada
Nat Genet 23:275-80. 1999....
Placebo-controlled trials in schizophrenia: are they ethical? Are they necessary?C Weijer
Dalhousie University, Halifax, Canada
Schizophr Res 35:211-8; discussion 227-36. 1999..While the use of a placebo control may be acceptable in carefully defined circumstances, in most cases the use of an active control in schizophrenia research is ethically and scientifically preferable...
Bioethics for clinicians: 16. Dealing with demands for inappropriate treatmentC Weijer
Mount Sinai Hospital, Toronto, Ont
CMAJ 159:817-21. 1998..Institutions should ensure that fair and unambiguous procedures for dealing with such cases are laid out in policy statements...
Bioethics for clinicians: 10. Research ethicsC Weijer
Mount Sinai Hospital, Toronto, Ont
CMAJ 156:1153-7. 1997..When difficulties arise, they should consult the existing literature and seek the advice of experts in research ethics...
Trust based obligations of the state and physician-researchers to patient-subjectsP B Miller
Department of Philosophy, University of Toronto, Ontario, Canada
J Med Ethics 32:542-7. 2006....
Hospital policy on appropriate use of life-sustaining treatment. University of Toronto Joint Centre for Bioethics/Critical Care Medicine Program Task ForceP A Singer
University of Toronto Joint Centre for Bioethics, Ontario, Canada
Crit Care Med 29:187-91. 2001..CONCLUSIONS: This article describes the key issues faced by the Task Force while developing its policy. It will provide a useful starting point for other groups developing policy on appropriate use of life-sustaining treatment...
A comparison of journal instructions regarding institutional review board approval and conflict-of-interest disclosure between 1995 and 2005A Rowan-Legg
Dr Anne Rowan Legg, Department of Pediatrics, IWK Health Centre, 5850 University Avenue, PO Box 9700, Halifax, Canada B3K6R8
J Med Ethics 35:74-8. 2009..To compare 2005 and 1995 ethics guidelines from journal editors to authors regarding requirements for institutional review board (IRB) approval and conflict-of-interest (COI) disclosure...
I need a placebo like I need a hole in the headCharles Weijer
Department of Bioethics, Dalhousie University, Halifax, Canada
J Law Med Ethics 30:69-72. 2002
Informing study participants of research results: an ethical imperativeConrad V Fernandez
Division of Pediatric Hematology/Oncology, Department of Pediatrics, IWK Health Centre and Dalhousie University, Halifax, Nova Scotia, Canada
IRB 25:12-9. 2003
Ethics of surgical training in developing countriesKevin M Ramsey
Cumberland Regional Health Care Centre, Amherst, Canada
World J Surg 31:2067-9; discussion 2070-1. 2007..All training programs need to develop a structured ethical review for international electives to protect their trainees and their patients from harm...
Lessons from everyday lives: a moral justification for acute care researchAndrew D McRae
Department of Bioethics, Faculty of Medicine, Dalhousie University, Halifax, Nova Scotia, Canada
Crit Care Med 30:1146-51. 2002..Our justification for emergency research also suggests additional protections for emergency research participants, including a stringent threshold for research risk, that still permit important research to proceed...
Meaningful work as due inducementCharles Weijer
Department of Philosophy, Talbot College, University of Western Ontario, London ON N6A 3K7, Canada
Theor Med Bioeth 26:431-5. 2005
Placebo trials and tribulationsCharles Weijer
Department of Bioethics, Dalhousie University, Halifax. charles.weijerAdal.ca
CMAJ 166:603-4. 2002
The return of research results to participants: pilot questionnaire of adolescents and parents of children with cancerC V Fernandez
Department of Pediatrics, IWK Health Centre, Halifax, Nova Scotia, Canada
Pediatr Blood Cancer 48:441-6. 2007..We examined the needs and attitudes of parents of children with cancer and of adolescents with cancer to the return of research results...
Providing research results to participants: attitudes and needs of adolescents and parents of children with cancerConrad Vincent Fernandez
Department of Pediatrics, IWK Health Centre, Dalhousie University, 5850 University Ave, PO Box 9700, Halifax, Nova Scotia, B3K 6R8, Canada
J Clin Oncol 27:878-83. 2009..There is an increasing demand for researchers to provide research results to participants. Our aim was to define an appropriate process for this, based on needs and attitudes of participants...
Obligations in offering to disclose genetic research resultsConrad V Fernandez
Dalhousie University, Canada
Am J Bioeth 6:44-6; author reply W10-2. 2006
Evaluating benefits and harms in intensive care researchCharles Weijer
Department of Philosophy, University of Western Ontario, 1151 Richmond Street, N6A 3K7, London, Ontario, Canada
Intensive Care Med 33:1819-22. 2007
A critical appraisal of protections for aboriginal communities in biomedical researchCharles Weijer
Department of Bioethics, Dalhousie University, Halifax, Canada
Jurimetrics 42:187-98. 2002..To explore how such a principle might be specified and operationalized, it reviews existing guidelines for protecting aboriginal communities and points out problems with these guidelines and areas for further work...
Therapeutic obligation in clinical researchCharles Weijer
Department of Bioethics, Dalhousie University
Hastings Cent Rep 33:3. 2003
The research subject as wage earnerJames A Anderson
Department of Bioethics, Dalhousie University, Halifax, Canada
Theor Med Bioeth 23:359-76. 2002..If we accept that paid research subjects are wage earners like any other, then the implications for changes to current practice are substantial...
Fiduciary obligation in clinical researchPaul B Miller
Department of Philosophy at the University of Toronto in Toronto, Ontario, Canada
J Law Med Ethics 34:424-40. 2006
Equipoise and the duty of care in clinical research: a philosophical response to our criticsPaul B Miller
University of Toronto, Toronto, Ontario, Canada
J Med Philos 32:117-33. 2007..However, recognizing that constructive contributions to the field ought to enjoy priority, we presently scrutinize the constructive dimension of their work. We argue that it is wanting in several respects...
Offering to return results to research participants: attitudes and needs of principal investigators in the Children's Oncology GroupConrad V Fernandez
Department of Pediatrics, IWK Health Centre, Dalhousie University, Halifax, Nova Scotia, Canada
J Pediatr Hematol Oncol 25:704-8. 2003..The authors determined current practice and attitudes and needs of researchers in establishing programs to return results to research participants...
Disclosure of the right of research participants to receive research results: an analysis of consent forms in the Children's Oncology GroupConrad V Fernandez
Department of Pediatrics, IWK Health Centre, Dalhousie University, Halifax, Nova Scotia, Canada
Cancer 97:2904-9. 2003..The current study examined the offer of return of research results by analyzing consent forms from 2 acute lymphoblastic leukemia studies of the 235 institutional members of the Children's Oncology Group...
Risk in emergency research using a waiver of/exception from consent: implications of a structured approach for institutional review board reviewAndrew D McRae
Department of Emergency Medicine, Queen s University, Kingston, Ontario, Canada
Acad Emerg Med 12:1104-12. 2005..The hypothesis was that component analysis could be used with a high degree of interrater reliability, and that the vast majority of emergency research would comply with a minimal-risk threshold...
U.S. Federal Regulations for emergency research: a practical guide and commentaryAndrew McRae
Department of Emergency Medicine, Queen s University, Kingston, Ontario, Canada
Acad Emerg Med 15:88-97. 2008..It explores the challenges for IRB review listed above, and offers potential solutions to these problems...
The balm of Gilead: is the provision of treatment to those who seroconvert in HIV prevention trials a matter of moral obligation or moral negotiation?Charles Weijer
Department of Philosophy, Talbot College, The University of Western Ontario, Canada
J Law Med Ethics 34:793-808. 2006..We outline an alternative approach to the problem based on moral negotiation...
The forum. The importance of context in international researchFern Brunger
Ethics Behav 12:371-2, 384-7. 2002
The ethics of placebo-controlled trialsCharles Weijer
N Engl J Med 346:382-3. 2002
Is clinical research and ethics a zero-sum game?Charles Weijer
Crit Care Med 33:912-3. 2005
When argument failsCharles Weijer
Dalhousie University
Am J Bioeth 2:10-1. 2002
Rehabilitating equipoisePaul B Miller
University of Toronto, Canada
Kennedy Inst Ethics J 13:93-118. 2003..CE sets out a standard for the social approval of research by institutional review boards. Viewed this way, FE and CE are not necessarily competing notions, but rather address complementary moral concerns...
Will the real Charles Fried please stand up?Paul B Miller
University of Toronto, Canada
Kennedy Inst Ethics J 13:353-7. 2003....
Waiver of consent for emergency researchAndrew D McRae
Ann Emerg Med 44:278-9; author reply 279-80. 2004
Ethical issues associated with the introduction of new surgical devices, or just because we can, doesn't mean we shouldSue Ross
Department of Obstetrics and Gynaecology, University of Calgary, Calgary AB
J Obstet Gynaecol Can 30:508-13. 2008....
Is the use of placebo controls ethically permissible in clinical trials of agents intended to reduce fractures in osteoporosis?Baruch A Brody
Center for Medical Ethics and Health Policy, Baylor College of Medicine, Houston, Texas, USA
J Bone Miner Res 18:1105-9. 2003..Active control trials are permissible and desirable if they can be designed and conducted in ways that overcome the interpretive difficulties often associated with such trials...
Importance of informed consent in offering to return research results to research participantsConrad V Fernandez
Med Pediatr Oncol 41:592-3. 2003
A critical history of individual and collective ethics in the lineage of Lellouch and SchwartzCharles M Heilig
Division of Reproductive Health, Centers for Disease Control and Prevention, Atlanta, GA 30341 371 7, USA
Clin Trials 2:244-53. 2005..Finally, the paper concludes with the observation that a systematic, comprehensive ethical framework must be identified to fulfill the intuitions behind individual and collective ethics...
Considerations and costs of disclosing study findings to research participantsConrad V Fernandez
Division of Pediatric Hematology and Oncology, Department of Pediatrics, IWK Health Centre Halifax, Nova Scotia
CMAJ 170:1417-9. 2004
