- Doctors should abstain from
engaging in research projects involving human subjects unless they are
satisfied that the hazards involved are believed to be predictable.
Doctors should cease any investigation if the hazards are found to
outweigh the potential benefits.
- In publication of the results of his
or research, the doctor is obliged to preserve the accuracy of the
results. Reports of experimentation not in accordance with the principles
laid down in this Declaration should not be accepted for publication.
- In any research on human beings,
each potential subject must be adequately informed of the aims, methods,
anticipated benefits and potential hazards of the study and the
discomfort, it may entail. He or she should be informed that he or she is
at liberty to abstain from participation in the study and that he or she
is free to withdraw his or her consent to participation at any time. The
doctor should then obtain the subject’s freely given informed consent,
preferably in writing.
- When obtaining informed consent
for the research project the doctor should be particularly cautious if the
subject is in a dependent relationship to him or her or may consent under
duress. In that case the informed consent should be obtained by a doctor
who is not engaged in the investigation and who is completely independent
of this official relationship.
- In case of legal incompetence,
informed consent should be obtained from the legal guardian in accordance
with national legislation. Where physical or mental incapacity makes it
impossible to obtain informed consent, or when the subject is a minor,
permission from the responsible relative replaces that of the subject in
accordance with national legislation.
- The research protocol should
always contain a statement of the ethical consideration involved and
should indicate that the principles enunciated in the present Declaration
are complied with.
(Ref: 18th World Medical Assembly,
Helsinki, Finland, 1964 and revised by the 29th World Medical Assembly, Tokyo,
Japan, 1975).
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