Particularidades de los ensayos clínicos ejecutados en las unidades de cuidados intensivos / Particularities of the clinical trials executed in the units of intensive cares
During the phase of planning of a clinical trial, keeping in mind the Good Clinical Practices and the ethical principles presented in the Statement of Helsinki, the elaboration of the Protocol of Investigation is carries out, where they are described clear and in detail the design, methodology and organization (practical considerations) of the study; the paragraphs of this document develop according to the specificities of the clinical trial. In this work the pecularities of the making of the Protocol of Investigation of a clinical trial were analyzed that involves the Units of Intensive Cares since their objective is to evaluate the efficacy and security of a Surfactante of national production in the Syndrome of Distress Respiratory Adult. It is concluded that in the studies in these units, they will participate a greater number of investigators, to request and to obtain the consent reported and to conserve the product in study in the unit(AU)