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It is a fundamental and universal requirement when conducting both clinical research and or trials that the main objective is and remains the same: to improve biological and medical humanistic conditions. This has been the norm for a greater part of a century. Countless scientists and diligent researchers have paved the way historically with vaccines for deadly diseases such as polio, small pox, whooping cough, measles, rabies and tetanus. As our world adjusts to ever changing components, so must
In 2014, Carl Elliott published an article about homeless people, many with severe mental illnesses, being recruited to test experimental drugs for the pharmaceutical industry (Elliott, Medium). The numbers of clinical trials that are held in United States are increasing every year and participants are needed to be involved in order to conduct these research. An ethical issue arises whether it is acceptable to pay the poor in order to test the safety of the new drug (Elliott and Abadie, Exploiting
Criteria for considering studies for this review We included any type of study design with data collection. There was no age restriction and we included studies looking at patients presenting with fever who were subsequently tested for dengue using both the Tourniquet test and Enzyme-Linked Immunosorbent Assay (ELISA). For this review: Dengue fever was considered: “Fever along with at least 2 of the following: headache, retroorbital pain, muscle pain, joint pain and rash. May be accompanied by
Definition and History of Evidence-Based Practice In the field of nurse anesthesia there are always clinical advances and an explosion of new information. So how does an anesthesia provider put all this new knowledge to good use in a clinical setting? Historically, nursing programs and medical schools have taught students to base their clinical decisions on expertise, experience, or single-sourced literature instead of a careful systematic review of all the available evidence (Pellegrini, 2006)