Page 10 - Ethical Guidelines for Conducting Research Studies Involving Human Subjects
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1.8.   Vulnerable  population  (Special  attention  should  be
                          provided by  the  investigator  in  development  of  research  studies
                          when the study involves the following category of subjects):

                                Children

                                Pregnant and Nursing Women

                                Mentally ill and mentally defective persons
                                Other vulnerable social and ethnic groups

                                Subjects in rural communities

                                Prisoner

                   02.   International Guidelines on Ethics in Health Research

                          In  1947,  the  Nuremberg  Code  the  first  International  document  on  the
                          ethics  of  medical  research  using  human  subjects  was  formulated.  The
                          Code was developed as a consequence of the trial of physicians who had
                          conducted  cruel  experiments  on  prisoners  and  detainees  during  the
                          Second  World  War.  The  code  emphasized  on  voluntary  consent.  The
                          Nuremberg Code is annexed (Annex-I).

                          Universal  Declaration  of  Human  Rights  adopted  by  the  United  Nations
                          General Assembly expressed concern about involuntary maltreatment. In
                          1966, the International Covenant on Civil and Political Rights stated, 'No
                          one  shall  be  subjected  to  torture  or  to  cruel,  inhuman  or  degrading
                          treatment or punishment. In particular, no one shall be subjected without
                          his consent to medical or scientific treatment'. (Article-7).

                          The  Declaration  of  Helsinki  is  considered  as  the  fundamental
                          document  in  the  field  of  ethics  in  medical  research.  This  document  was
                          adopted  by  the  World  Medical  Association  in  1964  and  subsequently
                          amended  in1975,  1983,  1989,  1996  and  2000.  The  Declaration  made  an
                          important     distinction   between    therapeutic    and    non-therapeutic
                          research and it made informed consent a central requirement for ethical
                          research, and  allow  for  surrogate  consent  when  the  research  participant
                          is minor and incompetent of giving consent. The   Declaration of Helsinki is
                          appended (Annex-2).

                          In 1979, the National Commission for the Protection of Human Subjects of
                          Biomedical  and  Behavioral  Research  wrote  their  report,  "Ethical
                          Principles  and  Guidelines  for  the  Protection  of  Human  Subjects  of
                          Research",  commonly  called  the  Belmont  Report.  In  this  report  the
                          Commission  identified  and  described  the  basic  ethical  principles  that
                          underlie  research  and  protect  the  certain  vulnerable  research
                          participant’s  e.g.  pregnant  women,  prisoners  and  children.  The
                          Commission  considered  the  boundaries  between  biomedical  and



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