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J Oncol Pract. 2011 Jul;7(4):267-70. doi: 10.1200/JOP.2011.000347.

A new look at informed consent for cancer clinical trials.

Author information

  • 1American Society of Clinical Oncology, Alexandria, VA; Community Oncology and Prevention Trials Research Group, Division of Cancer Prevention, National Cancer Institute, Bethesda, MD; Harvard Medical School; Masschusetts General Hospital, Boston, MA.

Abstract

Informed consent is fundamental to the conduct of clinical trials. Prospective participants need to be adequately informed and given the opportunity to ask questions and consult with relatives or friends without feeling pressured or rushed.

PMID:
22043194
PMCID:
PMC3140452
DOI:
10.1200/JOP.2011.000347
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