Editing 2726: Methodology Trial

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Treatments ''can'' be more effective on specific subgroups of the population; for example, an anti-cancer drug might only work against specific mutations that cause cancer. But any such result needs to have appropriate statistical significance and new subjects from that subgroup should be tested to ensure the result is repeated.
 
Treatments ''can'' be more effective on specific subgroups of the population; for example, an anti-cancer drug might only work against specific mutations that cause cancer. But any such result needs to have appropriate statistical significance and new subjects from that subgroup should be tested to ensure the result is repeated.
  
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The title text points out how the experiment has almost certainly violated some set of ethical standards, because one researcher offers what he believes to be genuine treatment to a large number of participants only for a third party (the offscreen speaker) to replace all his medicine with placebos, ultimately deceiving the patients. The title text implies that it was approved by a genuine Institutional Review Board (IRB), the group which decides whether a proposed experiment is ethical to perform. However they also have a "placebo IRB", presumably made up of people who have no qualifications to make such judgements well, or perhaps not made up of people at all, but simply a mechanism for generating random decisions.
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The title text points out how the experiment has almost certainly violated some set of ethical standards, because one researcher offers what he believes to be genuine treatment to a large number of participants only for a third party (the offscreen speaker) to replace all his medicine with placebos, ultimately deceiving the patients. The title text references that it was approved by a genuine Institutional Review Board (IRB), the group which decides whether a proposed experiment is ethical to perform. However they also have a "placebo IRB", presumably made up of people who have no qualifications to make such judgements well, or perhaps not made up of people at all, but simply a mechanism for generating random decisions.
  
 
However, such a methodology trial using all placebos wouldn't necessarily be unethical.  In addition to using a placebo, most studies are "double blind" meaning neither the patients nor the doctors/nurses treating them know who is getting the placebo and who is not; only the researchers conducting the study know.  This is so doctors/nurses cannot inadvertently let the patients know who is getting real medicine (by acting with remorse around patients they know are not being treated, or being more cheerful with patients they know who are).  It is considered perfectly ethical for doctors to give patients what they believe is medicine but is not (the placebo).  This is because without the double blind procedure it may not be possible to identify real medicines from ones that have no effect, and the impact of preventing real medicine from being used by millions is greater than the deceit towards the small number receiving a placebo in the experiment.  By extension it could be ethical to have the researcher conduct a trial with two placebos without knowing it.  For instance if the London team and the team in the comic were finding beneficial effects in new drugs that other researchers found had no effect (or finding other drugs didn't work when others had evidence they did) then it may be worth investigating if their shared methodology has the flaw demonstrated in the article.  That way regulatory agencies could exclude their flawed data when they make decisions on what drugs to approve, while the two teams could shift to a better methodology and return to contributing to medical science.
 
However, such a methodology trial using all placebos wouldn't necessarily be unethical.  In addition to using a placebo, most studies are "double blind" meaning neither the patients nor the doctors/nurses treating them know who is getting the placebo and who is not; only the researchers conducting the study know.  This is so doctors/nurses cannot inadvertently let the patients know who is getting real medicine (by acting with remorse around patients they know are not being treated, or being more cheerful with patients they know who are).  It is considered perfectly ethical for doctors to give patients what they believe is medicine but is not (the placebo).  This is because without the double blind procedure it may not be possible to identify real medicines from ones that have no effect, and the impact of preventing real medicine from being used by millions is greater than the deceit towards the small number receiving a placebo in the experiment.  By extension it could be ethical to have the researcher conduct a trial with two placebos without knowing it.  For instance if the London team and the team in the comic were finding beneficial effects in new drugs that other researchers found had no effect (or finding other drugs didn't work when others had evidence they did) then it may be worth investigating if their shared methodology has the flaw demonstrated in the article.  That way regulatory agencies could exclude their flawed data when they make decisions on what drugs to approve, while the two teams could shift to a better methodology and return to contributing to medical science.

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