An Overview of Clinical Trials in Chinese Medicine

https://doi.org/10.55529/jhtd23.14.18

Authors

  • Sudipto Ghosh Department of CSE, Bangladesh University of Business and Technology
  • Md. Tabil Ahammed Department of ECE, Khulna University of Engineering and Technology
  • Md. Shariar Rahman Oion Department of CSE, Bangladesh University of Business and Technology
  • Sahasa Debnath Department of CSE, Bangladesh University of Business and Technology

Keywords:

Traditional Chinese Medicine, Characteristics of TCM, Ethics Review, Drug Efficiency, Western Medicine

Abstract

To safeguard human participants and to scientifically assess the efficacy and safety
of a new medicine, a research protocol must be approved by an ethical committee before it
can begin. The first point to mention is that when it comes to clinical research, there are
fundamental differences between TCM and WM in three major areas: theoretical idea,
practice, and technique. combos made up of different elements It is necessary to conduct a
technical and ethical evaluation of the research process. These factors all influence safety
concerns, non-clinical research needs, drug quality requirements, enrolment, and efficacy
of clinical trials. In addition to ensuring that the medicine is lawful, a comprehensive
assessment must take into consideration the attributes of the already available TCM drug.

Published

2022-05-23

How to Cite

Ghosh, S. ., Ahammed, M. T. ., Oion, M. S. R. ., & Debnath, S. . (2022). An Overview of Clinical Trials in Chinese Medicine. Journal Healthcare Treatment Development, 2(03), 14–18. https://doi.org/10.55529/jhtd23.14.18