This paper discusses the ethical considerations of clinical and drug trials.
Written in 2008; 1,091 words; 4 sources; APA; $ 38.95
Paper Summary:
This paper discusses the ethics of the clinicians and the ethics of the participants. Additionally, the paper also discusses patient consent with regard to lower income, low literacy, and non-English speaking individuals. The paper concludes that study candidates should be honest and forthcoming when agreeing to participate, physicians should not be involved for their own glory and the clinical workers should remember that people are not just guinea pigs.
Outline:
Clinicians and Paid Participants
Informed Consent
Benefits of Clinical and Drug Trials
Conclusion
From the Paper:
"Every year, hundreds and even thousands of people loan their bodies and their health to be part of paid clinical trials. Some are desperate to help find the cures for cancer, Parkinson's disease, and Alzheimer's disease, or Lou Gehrig's disease, and some are looking for a way to make a few extra dollars. Unfortunately, some people are willing to become professional lab rats, travelling from study to study. The results of these clinical trials can then become skewed because the participants do not disclose that they are participating in a different study somewhere else."
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