Doing research on the ethics of doing research

Critical Care

Volumn 11, Issue 1, 2007, Pages

  Truog, Robert D ^a,b  

^a HARVARD MEDICAL SCHOOL   (United States)

^b BOSTON CHILDREN S HOSPITAL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CLINICAL PROTOCOL; CLINICAL RESEARCH; CRITICALLY ILL PATIENT; HEART SURGERY; HOSPITALIZATION; HUMAN; INFORMED CONSENT; INTENSIVE CARE; NEUROLOGIC DISEASE; NOTE; PRIORITY JOURNAL; QUALITATIVE RESEARCH; RECALL; REFUSAL TO PARTICIPATE; RESEARCH ETHICS; RETROGRADE AMNESIA; RISK BENEFIT ANALYSIS; VALIDATION PROCESS; CLINICAL TRIAL; ETHICS; INTENSIVE CARE UNIT; MEDICAL RESEARCH; PATIENT PARTICIPATION;

BIOMEDICAL RESEARCH; CLINICAL TRIALS; HUMANS; INFORMED CONSENT; INTENSIVE CARE UNITS; MENTAL RECALL; PATIENT PARTICIPATION;

EID: 34248185025     PISSN: 13648535     EISSN: 1466609X     Source Type: Journal    
DOI: 10.1186/cc5684     Document Type: Note

References (11)

1. Chenaud C, Merlani P, Luyasu S, Ricou B. Informed consent for research obtained during the intensive care unit stay. Crit Care 2006, 10:R170. 1794486, 17156444, 10.1186/cc5120.
2. Druml C, Singer EA. The European Directive: a further blow to science in intensive care medicine in Austria. Intensive Care Med 2004, 30:335. 10.1007/s00134-003-2089-0, 14685660.
3. Silverman HJ, Druml C, Lemaire F, Nelson R. The European Union Directive and the protection of incapacitated subjects in research: an ethical analysis. Intensive Care Med 2004, 30:1723-1729. 10.1007/s00134-004-2367-5, 15232680.
4. Lemaire F. The European Directive 2001/20 for clinical research: friend or foe?. Intensive Care Med 2006, 32:1689-1690. 10.1007/s00134-006-0386-0, 17019542.
5. Truog RD. Will ethical requirements bring critical care research to a halt?. Intensive Care Med 2005, 31:338-344. 10.1007/s00134-004-2480-5, 15526188.
6. Chenaud C, Merlani P, Ricou B. Informed consent for research in ICU obtained before ICU admission. Intensive Care Med 2006, 32:439-444. 10.1007/s00134-005-0059-4, 16477413.
7. National Commission for the Protection of Human Subjects of Biomedical and Behavioral Research The Belmont Report: Ethical Principles and Guidelines for the Protection of Human Subjects of Research 1979, Washington, DC: Government Printing Office, National Commission for the Protection of Human Subjects of Biomedical and Behavioral Research.
8. Gammelgaard A, Mortensen OS, Rossel P. Patients' perceptions of informed consent in acute myocardial infarction research: a questionnaire based survey of the consent process in the DANAMI-2 trial. Heart 2004, 90:1124-1128. 10.1136/hrt.2003.021931, 15367504.
9. Williams BF, French JK, White HD. Informed consent during the clinical emergency of acute myocardial infarction (HERO-2 consent substudy): a prospective observational study. Lancet 2003, 361:918-922. 10.1016/S0140-6736(03)12773-0, 12648970.
10. Harvey SE, Elbourne D, Ashcroft J, Jones CM, Rowan K. Informed consent in clinical trials in critical care: experience from the PAC-Man Study. Intensive Care Med 2006, 32:2020-2025. 10.1007/s00134-006-0358-4, 17019555.
11. Annane D, Outin H, Fisch C, Bellissant E. The effect of waiving consent on enrollment in a sepsis trial. Intensive Care Med 2004, 30:321-324. 10.1007/s00134-003-2065-8, 14714106.