Placebo Effect For Research Ethics

Decent Essays
Both doctors think using the placebo effect for research is ethical, because the patient knows they could be given a placebo and signs a consent form. They think it is a great way to determine if a medicine actually has effects, or if its only because the patient thinks it should work. Natasja van Oppen is involved in a clinical trial for thyroid disorders, which involves the use of the placebo effect. The patients are all given a blue pill, some are placebos and others contain the medicine. The trial is still going and it is a very slow process so the results will be available in six

Related Documents

  • Superior Essays

    Henrietta Lacks Critique

    • 1916 Words
    • 8 Pages

    Even though informed consent was still in its infancy, doctors had every right to use Lacks’s cells for their research. John Hopkins Hospital, where Ms. Lacks received her care, did not have Institutional Review Board (IRB) to govern and approve their research protocols. I agree with the doctors in wanting to develop a cure for various illnesses. My only issue this particular point is that they didn’t inform her. Even though they had every right to not tell her, I still believe they would be courteous and have the decency to tell her that they believe her cells can change the…

    • 1916 Words
    • 8 Pages
    Superior Essays
  • Improved Essays

    They knew how to contact us! If Dr. Gey wasn't dead, I think I would have killed him myself” (169). We should not make someone feel like this anymore. Therefore, medical research should not be done without the patient’s informed consent even if research proves invaluable for humankind because everyone must have their rights to select what they want to do with their…

    • 1099 Words
    • 5 Pages
    Improved Essays
  • Great Essays

    HIPAA Case Study

    • 1162 Words
    • 5 Pages

    Only the doctor should examine the results and give the recommendations based on the findings. She should have kept communications with the patient private and within the facility. She infringed on the Patent’s Right to privacy. This is because patient’s confidentiality must be protected by all those who are part of health services.…

    • 1162 Words
    • 5 Pages
    Great Essays
  • Improved Essays

    It wasn’t ethical to put all the subjects on an experimental drug before knowing about any possible negative side effects. I say that because Dr. Sayer and the other nurses were unaware of hardly any effects. They…

    • 379 Words
    • 2 Pages
    Improved Essays
  • Improved Essays

    Ethics of Patient Treatment The book The Immortal Life of Henrietta Lacks is a true story based on Henrietta Lacks, who was a patient at John Hopkins in the 1950’s. Treatment of African Americans in the 1950’s was very cruel and inhuman in the medical field and was fueled by racial stigmas and socioeconomic status. In the 1950’s African Americans were also targeted because of their socioeconomic status and ethnicity to participate in medical research such as the very cruel Tuskegee syphilis experiment. Henrietta’s cells were later stolen and then sold for medical research which started a billion-dollar industry that Henrietta’s family never saw a dime of.…

    • 1995 Words
    • 8 Pages
    Improved Essays
  • Improved Essays

    The main points of ethical standard 8.07 Deception in Research are: 1. Not using deceptive research practices unless the use is justified and effective non deceptive techniques are not feasible. 2. Avoiding deceptive research that causes physical pain or severe emotional distress.…

    • 295 Words
    • 2 Pages
    Improved Essays
  • Improved Essays

    Among medical researchers as well as clinicians, the prevailing opinion is that it is unethical to mislead patients by prescribing a placebo. This belief has been sanctioned by a recent policy published by the American Medical Association. Although placebos can be shown to be always harmless, and frequently effective, physicians are now prohibited from administering them in medical practice. In the article “A Duty to Deceive: Placebos in Clinical Practice” by Bennett Foddy, he argues that the deceptive administration of placebos is not subject to the same moral objections that face other forms of deception in clinical practice and medical research. Although deception is normally objectionable on the grounds that it limits autonomy and breaches…

    • 1017 Words
    • 5 Pages
    Improved Essays
  • Great Essays

    Ethics This essay will discuss the ethical safeguards for clinical research that may not apply to evidence-based projects. Additionally, this essay will discuss ethical controversies related to two ethical exemplars. In conclusion, patients’ ethical responsibility in improving healthcare will be explored. Ethical Safeguards Clinical research involves the study of investigational analysis of data or experiments that involve humans.…

    • 1356 Words
    • 6 Pages
    Great Essays
  • Decent Essays

    Jeffrey, I enjoyed reading your post and understanding your point of view on the topic. Evaluators deal with ethical conflicts that most social scientists and other researchers seldom experience while conducting research (Posavac,2011). I agree that informed consent and confidentiality are very important are interdependent and necessary, one for the effective functioning of the other. Ethical research is imperative for numerous reasons and has driven organizations and agencies to develop and adopt ethical principles to protect patient volunteers, staff and to preserve the integrity of the science, program and research. There are many ways harm can be done to those who are participating in the program and the staff.…

    • 244 Words
    • 1 Pages
    Decent Essays
  • Great Essays

    When faced with an ethical medical question, there is almost always a “right” choice; however, it can be hard to see the possible ramifications of one’s choices. There is a lot of controversy surrounding researcher behavior in trials, especially those involving new drugs. There are certain protocols that must be followed when testing a research drug, and straying from these guidelines can hurt not only the specific research project, but the entirety of one’s career. In order to understand the importance of adhering to Phase 1 research trial guidelines, one must first understand the purpose of Phase 1 trials, the importance of protocol and patient-physician relationships, and the opposing viewpoints. This paper will analyze a scenario in which…

    • 2448 Words
    • 10 Pages
    Great Essays
  • Improved Essays

    Ethical Concerns Experimental design is a field whereby ethical concerns are almost always a top priority. Although most individuals see ethical norms as common sense, they often vary from culture to culture and there can be discrepancies in the interpretation even by members within a certain cultural group. Furthermore, it is vital to determine any potential ethical concerns contained within an experiment and address those concerns in order to reduce their potential impact on the results. The first potential ethical concern that may be encountered during our experiment is an experimenter either intentionally or accidentally falsifying, fabricating or misrepresenting the data that is collected from the test subjects.…

    • 713 Words
    • 3 Pages
    Improved Essays
  • Improved Essays

    I believe that a research should not gain informed consent from someone who does not have the mental capability to do so. Even if it could POSSIBlY cure them, they have no idea of the risk factors of the actual procedure. If someone has the power of attorney and is looking out for the best interest…

    • 564 Words
    • 3 Pages
    Improved Essays
  • Superior Essays

    Many patients will be prescribed drugs and they will believe that the drugs will work but the patient does not improve because of the actual chemical components of the drug. An article written in an APA magazine says, “Studies have shown that people with mild depression that take antidepressants, do not do significantly better than using placebos” (Smith36). Often times prescription drugs act as a placebo effect, the chemicals in the drugs are not healing them, but the patient believe that it…

    • 1074 Words
    • 5 Pages
    Superior Essays
  • Improved Essays

    Essay On Antidepressants

    • 1657 Words
    • 7 Pages

    Subjects experiencing adverse effects guessed that they were given the real drug and therefore have a higher placebo effect than those given placebo since they “know” that they have been given the drug. Patients given antidepressants are also more likely to become depressed again after treatment compared with other treatments such as placebo Andrews et al., 2012; Babyak et al., 2000; Dobson et al., 2008. One possibility is therefore to prescribe placebos since they are almost as effective as antidepressants, but with fewer side-effects. Studies indicate that some doctors actually do prescribe placebos Raz et al., 2011; Tilburt, Emanuel, Kaptchuk, Curlin, & Miller, 2008. This is however a question of ethics.…

    • 1657 Words
    • 7 Pages
    Improved Essays
  • Superior Essays

    There are certain ethical considerations that should be considered by the researcher at the time of conducting research. Some of the key ethical considerations are as follows: 3.7.1 Validity and Credibility The investigator ensures that all the information is gathered are from valid and trustworthy places so that issues can be evaded. Moreover, attaining accurate data would make it expedient for the investigator to provide confirmation to the arguments in the research. In addition, consistency and validity is also imperative because it minimises the probability of utilising of immaterial info, which makes the research meaningless and vague (Y.k.singh, 2010).…

    • 1667 Words
    • 7 Pages
    Superior Essays