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      Ethical tradeoffs in trial design: case study of an HPV vaccine trial in HIV-infected adolescent girls in lower income settings.

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          Abstract

          The Declaration of Helsinki and the Council of the International Organization of Medical Sciences provide guidance on standards of care and prevention in clinical trials. In the current and increasingly challenging research environment, the ethical status of a trial design depends not only on protection of participants, but also on social value, feasibility, and scientific validity. Using the example of a study assessing efficacy of a vaccine to prevent human papilloma virus in HIV-1 infected adolescent girls in low resource countries without access to the vaccine, we compare several trial designs which rank lower on some criteria and higher on others, giving rise to difficult trade-offs. This case demonstrates the need for developing more nuanced guidance documents to help researchers balance these often conflicting criteria.

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          Author and article information

          Journal
          Dev World Bioeth
          Developing world bioethics
          Wiley-Blackwell
          1471-8847
          1471-8731
          Aug 2013
          : 13
          : 2
          Affiliations
          [1 ] Harvard School of Public Health – Center for Biostatistics in AIDS Research, 651 Huntington Avenue, Boston, MA 02115, USA. lindsey@sdac.harvard.edu
          Article
          NIHMS448599
          10.1111/dewb.12028
          3716837
          23725055
          479d72ee-94fc-4b60-9e43-26cc0820f23b
          History

          clinical trials,public health,research ethics,standard of care,vaccines

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