Clinical research XXIV. From clinical judgment to ethics in research on humans

Main Article Content

Marcela Pérez-Rodríguez
Lino Palacios-Cruz
Rodolfo Rivas-Ruiz
Juan O Talavera

Keywords

Bioethics, Informed consent, Beneficence

Abstract

Bioethics in research is an essential part of the structured review process of an article and it is based on three fundamental principles: respect for persons, beneficence and justice. In addition to not providing valid knowledge, a research with inadequate design, execution and statistical analysis is not ethical either, since these methodological deficiencies will produce information that will not be useful and, therefore, the risks that the participants were exposed to will have been in vain. Beyond scientific validity, there are other aspects that outline if an investigation is ethical, such as the clinical and social value of a study, a fair selection of participants, favorable risk-benefit balance, an independent review, the informed consent and respect for participants and potential participants. Throughout the article here presented, the documents that profile the behavior of investigators to protect the participants, such as the Declaration of Helsinki, the national regulations that rule us and the differences between research without risk, with minimal risk and with greater than minimal risk are discussed. That like in daily life, behavior in research involving human participants must be self-regulated , ie , people with knowledge of the existence of the law discover that the man is outside the realm of nature where work is done under the necessity of natural causality , and falls within the scope of the will; only if the man is free to decide their actions may be a law regulating their action.
Abstract 288 | PDF (Spanish) Downloads 1257

References

Yarborough M. Taking steps to increase the trustworthiness of scientific research. FASEB J. 2014 Jun 13. pii: fj.13-246603

 

Belhekar MN, Bhalerao SS, Munshi RP. Ethics reporting practices in clinical research publications: A review of four Indian journals. Perspect Clin Res. 2014;5(3):129-33. Disponible en http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4073550/

 

Dingemann J, Dingemann C, Ure B. Failure to report ethical approval and informed consent in paediatric surgical publications. Eur J Pediatr Surg. 2011;21 (4):215-9.

 

Marwick C. Philosophy on Trial: Examining ethics of Clinical Investigations. JAMA. 1988;(6)260;749-51.

 

Norma oficial mexicana NOM-012-SSA3-2012, que establece los criterios para la ejecución de proyectos de investigación para la salud en seres humanos. Diario Oficial de la Federación del 4 de enero de 2013. Disponible en http://dof.gob.mx/nota_detalle.php?codigo=5284148&fecha=04/01/2013

 

Reglamento de la Ley General de Salud en Materia de Investigación para la Salud. Diario Oficial de la Federación del 2 de abril de 2014. Disponible en http://www.salud.gob.mx/unidades/cdi/nom/compi/rlgsmis.html

 

Emanuel EJ, Wendler D, Grady C. What makes clinical research ethical? JAMA. 2000;283(20):2701-11.

 

Connolly SJ, Ezekowitz MD, Yusuf S, Eikelboom J,Oldgren J. Dabigatran versus warfarin in patients with atrial fibrillation. N Engl J Med. 2009;361: 1139-51.

 

Kant I. Fundamentación de la metafísica de las costumbres. [traducción de Manuel García Morente]. Edición digital basada en la sexta edición. Madrid, España: Espasa-Calpe; 1980.