Review on Ethics in Research – Homoeopathic Perspective

A. Sahoo, B. Damodaran, C. Nayak, Umakant Prusty, Priyanka Ghosh
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Abstract

Abstract Ethics is a moral principle that governs a system. Research ethics may be defined as doing what is morally and legally right in research. Despite dealing with human beings, homoeopathy research deals with human clinical, pre-clinical (drug proving) trials, preclinical animal studies, veterinary studies and plant studies that demand varied ethical strategies. The importance of ethics in medical research is mandated to avoid adverse events before, during and after the trials. Ethics in medical practice and medical research is based on Nuremberg's Code and Declaration of Helsinki. The two major guidelines in the homoeopathic medical research publications are Reporting data on Homeopathic treatments (RedHot): A supplement to Consolidated Standards for Reporting Trials (CONSORT) for clinical trials and Reporting Experiments in Homeopathic Basic Research (REHBaR). This article discusses the evolution of ethics in medical research, principles of ethics, components to be considered pre-trial, during and post-trial. The evolution of strategies based on the principles of ethics in medical research is correlated.
研究中的伦理学综述-顺势疗法的视角
伦理是支配一个制度的道德原则。研究伦理可以定义为在研究中做道德和法律上正确的事情。尽管研究对象是人类,但顺势疗法研究涉及人类临床、临床前(药物证明)试验、临床前动物研究、兽医研究和植物研究,这些都需要不同的伦理策略。医学研究中伦理的重要性在于避免试验前、试验中和试验后的不良事件。医学实践和医学研究中的道德规范以《纽伦堡法典》和《赫尔辛基宣言》为基础。顺势疗法医学研究出版物的两个主要指南是顺势疗法治疗数据报告(RedHot):临床试验报告综合标准(CONSORT)的补充和顺势疗法基础研究报告实验(REHBaR)。本文讨论了医学研究中伦理的演变、伦理原则、审前、审中和审后应考虑的组成部分。基于医学研究伦理原则的策略演变是相互关联的。
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