• 1
    Warnock M. Informed consent: a publisher's duty. In: DoyalL, TobiasJS, editors. Informed consent in medical research. London: MBJ Books; 2001. p. 12930.
  • 2
    Beauchamp TL, Childress JF. The principle of respect for autonomy. In: BeauchampTL, ChildressJF, editors. Principles of biomedical ethics. 3rd ed. New York: Oxford University Press; 1989. p. 749.
  • 3
    Criscione LG, Surgarman J, Saunders L, Pisetsky DS, St Clair WE. Informed consent in a clinical trial of a novel treatment for rheumatoid arthritis. Arthritis Rheum (Arthritis Care Res) 2003; 49: 3617.
  • 4
    Snowdon C, Garcia J, Elbourne D. Making sense of randomisation: responses of parents of critically ill babies to random allocation of treatment in a clinical trial. Soc Sci Med 1997; 45: 133755.
  • 5
    Sutherland HJ, Lockwood GA, Till JE. Are we getting informed consent from patients with cancer? J R Soc Med 1990; 83: 43943.
  • 6
    Featherstone K, Donovan JL. Why don't they just tell me straight, why allocate it? The struggle to make sense of participating in a randomised controlled trial. Soc Sci Med 2002; 55: 70919.
  • 7
    Baker MT, Tabu HA. Readability of informed consent forms for research in a Veterans Administration Medical Center. JAMA 1983; 250: 26468.
  • 8
    Priestley KA, Campbell C, Valentine CB, Denison D, Buller NP. Are patient consent forms for research patients easy to read? BMJ 1992; 305: 12634.
  • 9
    Hewlett S. Consent to clinical research: adequately voluntary or substantially influenced? J Med Ethics 1996; 22: 2327.