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Editorial
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Volume 351:1250-1251 September 16, 2004 Number 12
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Clinical Trial Registration: A Statement from the International Committee of Medical Journal Editors
Catherine De Angelis, M.D., M.P.H., Jeffrey M. Drazen, M.D., Frank A. Frizelle, M.B., Ch.B., M.Med.Sc., F.R.A.C.S., Charlotte Haug, M.D., Ph.D., M.Sc., John Hoey, M.D., Richard Horton, F.R.C.P., Sheldon Kotzin, M.L.S., Christine Laine, M.D., M.P.H., Ana Marusic, M.D., Ph.D., A. John P.M. Overbeke, M.D., Ph.D., Torben V. Schroeder, M.D., D.M.Sc., Hal C. Sox, M.D., and Martin B. Van Der Weyden, M.D.

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Altruism and trust lie at the heart of research on human subjects. Altruistic individuals volunteer for research because they trust that their participation will contribute to improved health for others and that researchers will minimize risks to participants. In return for the altruism and trust that make clinical research possible, the research enterprise has an obligation to conduct research ethically and to report it honestly. Honest reporting begins with revealing the existence of all clinical studies, even those that reflect unfavorably on a research sponsor's product.

Unfortunately, selective reporting of trials does occur, and it distorts the body of evidence . . . [Full Text of this Article]


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Clinical Trial Registration
Grass G., Reveiz L., Cardona A. F., Ospina E. G., Kulvichit K., Kulwichit W., Lumbiganon P.
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N Engl J Med 2005; 352:198-199, Jan 13, 2005. Correspondence

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