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Public and patient usage and expectations for clinical trial registries

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Clinical Trial Registries

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References

  1. De Angelis C, Drazen JM, Frizelle FA et al. Clinical trial registration: a statement from the International Committee of Medical Journal Editors. Available at www.icmje.org (Accessed: 29 January 2006)

    Google Scholar 

  2. Hayward R, Kent D, Vijan S, Hofer TP (2005) Reporting clinical trial results to inform providers, payers and consumers. Health Affairs 24: 1571–1581

    Article  PubMed  Google Scholar 

  3. Fisher CB (2006) Clinical trial results databases: Unanswered questions. Science 311: 180–181

    Article  PubMed  CAS  Google Scholar 

  4. Office of the New York State Attorney General Eliot Spitzer. Major pharmaceutical firm concealed information. Available at http://www.oag.state.ny.us/press/2004/jun/jun2b_04.html (Accessed 17 March 2005)

    Google Scholar 

  5. United States Food and Drug Administration. Section 113 Food and Drug Administration Modernization Act of 1997. Available at: http://lhncbc.nlm.nih.gov/clin/113.html (Accessed 8 February 2006)

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  6. Manheimer E, Anderson D (2002) Survey of public information about ongoing clinical trials funded by industry: evaluation of completeness and accessibility. Br Med J 325: 528–531

    Article  Google Scholar 

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© 2006 Birkhäuser Verlag Basel/Switzerland

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Getz, K. (2006). Public and patient usage and expectations for clinical trial registries. In: Foote, M. (eds) Clinical Trial Registries. Birkhäuser Basel. https://doi.org/10.1007/978-3-7643-7583-6_4

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