This week's blog post will be an addition to my first mini paper on the topic of human experimentation, with respect to drug trials. I came across an article that was similar to what I discussed in the paper, titled “Drug Trial Participants Not Fully Informed About Placebos,” which discussed one of the topics I covered in the paper. In this article, the author argues that patients should be informed about the placebo, as well as the trial drug. He stated that in most cases, the placebo is overlooked altogether, even though they often have some side effects. The “placebo effect”, as it is often referred to, can indeed change people’s symptoms, and sometimes they go away altogether. According to medical researchers at Southampton University, “they recommend that different ways of describing placebos and their potential effects should now be tested, not only where such information appears in leaflets, but also in how it is communicated by researchers and administrators who have personal contact with participants in drug trials.”
I think this is an important distinction to make, as the “placebo effect” does exist. The doctors are so interested in promoting the trial drug and making sure the patient is fully informed that they tend to overlook what the placebo can do. These patients may believe they were on the drug the whole time, when in reality their body was reacting to the psychological effect of taking the placebo. Informed consent must go both ways; the patient should know when there is a trial drug that has some potentially negative side effects, but they should also be aware of what might come from taking the placebo, if that is the case.
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