Preview

Lack Of Informed Consent In Clinical Research

Good Essays
Open Document
Open Document
2387 Words
Grammar
Grammar
Plagiarism
Plagiarism
Writing
Writing
Score
Score
Lack Of Informed Consent In Clinical Research
Research Ethics

The term ethics dates back hundreds of years, and today the meaning still holds true. Ethics is simply doing the right thing, which involves acting in the right spirit, out of an unwavering respect and concern for one another. In learning about the health profession one of the very first things a student is introduced to is ethics. What is considered morally right? What ethical decision-making process leads a person to a particular decision? In clinical research, ethics plays a very critical role, as medical professionals and researchers heavily rely on their ethics and the ethical decision- making process to produce the best caring response for patients. One way to guarantee that patients involved in clinical research are
…show more content…
Informed consent is essentially when the patient or participant grants permission with the knowledge of all possible consequences, risks, and benefits that are associated with the procedure being performed. It is critically important to obtain informed consent from all clinical participants involved, as this helps all medical professionals and research to perform their duties knowing full well that they are taking into account the needs and wishes of the participants. There is no guessing involved as to what the participants would want to do in regards to the procedure because everything is outlined within the informed consent (Purtilo & Doherty, n.d.p. 250). There are various factors to informed consent some of which include, the health or value of what the research will hold for all participants involved. It must also show the validity of the research to ensure it is scientifically sound. Informed consent also provides the risks associated with the research being performed, and along with that the research must be approved and reviewed and could possibly be terminated. Informed consent fully supports the principle of patient autonomy by fully allowing any patient or research participant to decline treatment or procedures (Emanuel, …show more content…
One common misconception is that animals are so different from humans that research is unconnected. However, one of the reasons why animal research is so essential in scientific discovery is because animals actually share very similar biologically. We share the same organs and these bodily processes work the same way in both humans and animals, so it is important to see how certain treatment, drugs and diseases affect animals because it gives us a clue as to how the human body would respond. Another misconception is that medicine that works in people are toxic to animals and vise versa. An example of this misconception is that penicillin is toxic to guinea pigs; however, studies have shown that much like humans, penicillin is only toxic in extreme doses. In a case like the one involving penicillin, this study further proves that by testing this antibiotic on animals first we can discover what the recommended doses are and how much is needed to treat an infection. Lastly, the misconception that animal research is inconclusive and has not made any real contributions in the medical field is simply false. Again, animal research has contributed greatly toward the medical field as the discovery of insulin was tested first on dogs who were diabetic and the results were so promising that insulin was introduced as the go to treatment for diabetes among people.

You May Also Find These Documents Helpful

  • Good Essays

    Healthcare professionals should understand the basics of informed consent, they should also never fall short of relaying the information in detail, so it would allow the patient or guardian to make an informed judgement that would be in the care seeker’s best interest. As healthcare providers, our society as a whole trusts their opinion and holds their opinion at a high regard, which is why professional standards forces them to inform the society, in this case their patients, of all the possible treatments and the pros and cons that follow the treatment, in order to bring the individual to their standard of status quo. Physicians have a series of questions to ask themselves, which assist them in justifying that the patient has all the information necessary to…

    • 1006 Words
    • 5 Pages
    Good Essays
  • Satisfactory Essays

    Henritta Lacks Paper

    • 446 Words
    • 2 Pages

    Informed consent is a legal procedure to ensure that a patient or client knows all of the risks and costs involved in a treatment. Up to 1947, the thought of informed consent hadn’t even crossed anyone’s mind. In 1947, the Nuremberg trials were held wherein 7 Nazi scientist were convicted of conducting unthinkable tests on Jewish subjects. This marked the first time informed consent entered anyone’s conscience. It still wasn’t law. It was just an ethical code which had no legal bindings. Then ten years later, when scientist Southman was injecting HeLa into patients’ bodies without telling them how dangerous it was and some of them died and an investigation ensued. This caused a division between people and doctors. Some doctors decided against informed consent because it would interfere with their research practices.…

    • 446 Words
    • 2 Pages
    Satisfactory Essays
  • Powerful Essays

    Regarding informed consent, the guidelines APA and BPS both advise that informed consent are to be obtained before the experiment. The APA goes further by detailing what information are to be informed to the subjects, such as the purpose of the research, the right to decline, consequences, confidentiality, incentives and who to question with regards to the experiment.…

    • 1203 Words
    • 5 Pages
    Powerful Essays
  • Good Essays

    Leonard Thompson Biography

    • 1042 Words
    • 5 Pages

    Scientists are constantly looking for new medical advances that they hope will save people’s lives and often turn to animals as the optimal resource for testing new ideas and products. These animals range from rats and mice to dogs and monkeys. On top of varying animals, the tests they run fluctuate from simply checking the effectiveness of a medicine already in use to testing an entirely new form of treatment. However, there have beens years of controversy over the morality of using animals as the test subjects.…

    • 1042 Words
    • 5 Pages
    Good Essays
  • Better Essays

    In The Immortal Life of Henrietta Lacks by Rebecca Skloot mentions animal experimentation. Different kinds of animals are used in many different experiments. Most experiments are used to help humans more than to help animals. Animal experimentation should not happen because most of the time, experiments can lead to animal cruelty. Cloning is one example of an experiment.…

    • 991 Words
    • 4 Pages
    Better Essays
  • Satisfactory Essays

    As a clinical research nurse, it is my responsibility to ensure that all of my patients (or subjects) submit a signed and dated informed consent (IC) form prior to enrollment in a study. The Food and Drug Administration (FDA) requires that all clinical trials or study sponsors (pharmaceutical manufacturer of the study drug) maintain proof of IC for each subject, in every trial, without exception in their respective trial master file (TMF). Potential barriers for participants in clinical research studies might be patients or subjects who are uneducated, and or, patients who are not able to assure his or her health care provider that they fully understand information that is provided, and IC may not be obtained. The NIH defines consent capacity as an "adult's ability to understand information relevant to making an informed, voluntary decision to participate in research." This information includes a description of the study, its potential risks and benefits, the right to give voluntary consent, the right to withdraw from the study, anonymity, confidentiality, and ways to lessen any risks. However, many people do not understand these components of an informed consent for a variety of reasons. These include people with "mental disorders, neurological disorders such as stroke or dementia, metabolic impairment,…

    • 535 Words
    • 3 Pages
    Satisfactory Essays
  • Good Essays

    Consent also has a legal angle. Patients have the right to decide about what they do or what others can do to their lives and their bodies. Therefore, obtaining consent is necessary for anything other than a routine physical examination and investigation. Informed consent prior medical intervention protects the doctor and the hospital in which he or she works from certain forms of litigation, because the medical intervention was legal, and carried out after authorization by the patient. However, legal protection of the informed consent does not protect the doctor in case of errors and malpractice. The primary care physician obtained informed consent from Mrs. R and I also take the patient’s consent for conducting the interview since any act done without permission, is considered as medical battery. Additionally,…

    • 669 Words
    • 3 Pages
    Good Essays
  • Good Essays

    Qualitative Study Nursing

    • 1625 Words
    • 7 Pages

    Fundamental to ethical research is respect for the autonomy of research participants. Autonomy refers to the right of an individual to make decisions about those things that affect them. In the context of research, participants should have the opportunity to make an informed decision about whether to participant in research or not. For consent to be valid it should be informed, it should be voluntary and the person giving consent should have the capacity to give that consent (Beauchamp and Childress,…

    • 1625 Words
    • 7 Pages
    Good Essays
  • Good Essays

    Informed Consent

    • 736 Words
    • 3 Pages

    Nursing Implications Regarding Health Literacy and Informed Consent Roughly 90 million Americans have low health literacy. However, the responsibility of improving health literacy does not fall solely on the patient but also on health care organizations, including healthcare professionals (Mahadevan, 2013). More specifically, nurses have a responsibility to assess a patient's literacy level in order to provide appropriate patient care, education and counseling.…

    • 736 Words
    • 3 Pages
    Good Essays
  • Good Essays

    Informed Consent

    • 848 Words
    • 3 Pages

    Informed consent is obtained by a legally competent person, who voluntarily accepts or declines the consent after being informed of the treatment including side effects, adverse effects.(Ref 1,2) Many people are frightened by unfamiliar medical procedures and interventions and may thus want to back off from any treatment. This decision should be respected, and the client should not be forced into taking any of these medication or treatment. Rather the nurse can educate them to the best of…

    • 848 Words
    • 3 Pages
    Good Essays
  • Good Essays

    Medical Law and Ethics

    • 1706 Words
    • 7 Pages

    Informed consent involves the patient’s right to receive all information relative to his or her condition and to make a decision regarding treatment based upon that knowledge.…

    • 1706 Words
    • 7 Pages
    Good Essays
  • Good Essays

    Essay About Animal Testing

    • 1173 Words
    • 5 Pages

    The experimentation on animals may be an iniquitous act to some people; conversely, some people might see it as a tool used to save many lives. Animal experimentation in the medical field has been useful in many ways. Scientists are able to take information learned from animals and make educated guesses about the human body’s functions and determine a person’s reaction to a drug.…

    • 1173 Words
    • 5 Pages
    Good Essays
  • Better Essays

    In the article by Martindale, Chambers, and Thompson, we learn that informed consent and confidentiality. A person should be informed of their right to confidentiality and the treatment they are consenting to in the therapeutic relationship. This study is significantly important because we are shown that there has been not very much previous research done on how well we manage consent, how informed the patient is, how honest they are, and what they actually know about the policies of the provider.…

    • 987 Words
    • 4 Pages
    Better Essays
  • Good Essays

    When it comes to the topic of animal testing, most of us will readily agree that it is a debatable topic. Where this agreement usually ends, however, is on the question of whether it helps researchers to find new drugs and treatments suitable for humans. Whereas some are convinced that it does help researchers find new drugs and treatments, others maintain that some drugs tested on animals may never actually be useful or even safe for human consumption. In my own view the results of animals testing are unreliable because animals and humans are not genetically or anatomically alike to one another.…

    • 566 Words
    • 3 Pages
    Good Essays
  • Powerful Essays

    Informed Consent

    • 2404 Words
    • 10 Pages

    The principles of informed consent were laid down in the context of American medical practice in a landmark case dating from the 1914: Schloendorf vs New York Hospital Society (Bennett). Following a surgical procedure was carried out a patient who had previously refused the surgery, the judge ruled that every human being of adult years and of sound mind has a right to determine what shall be done with his own body.…

    • 2404 Words
    • 10 Pages
    Powerful Essays