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[Guidelines for post-marketing research on clinical effectiveness of Chinese patent medicines].
Wang, Zhi-Fei; Xie, Yan-Ming; Tang, Jian-Yuan; Zhang, Jun-Hua; Sun, Xin; Yang, Zhong-Qi.
Afiliação
  • Wang ZF; Institute of Basic Research in Clinical Medicine, China Academy of Chinese Medical Sciences Beijing 100700, China.
  • Xie YM; Institute of Basic Research in Clinical Medicine, China Academy of Chinese Medical Sciences Beijing 100700, China.
  • Tang JY; Affiliated Hospital of Chengdu University of Traditional Chinese Medicine Chengdu 610075, China.
  • Zhang JH; Evidence-based Medicine Center, Tianjin University of Traditional Chinese Medicine Tianjin 301617, China.
  • Sun X; Chinese Cochrane Center, West China Hospital, Sichuan University Chengdu 610041, China.
  • Yang ZQ; First Affiliated Hospital of Guangzhou University of Chinese Medicine Guangzhou 510407, China.
Zhongguo Zhong Yao Za Zhi ; 49(3): 842-848, 2024 Feb.
Article em Zh | MEDLINE | ID: mdl-38621888
ABSTRACT
Due to the lack of specialized guidance, the post-marketing research on clinical effectiveness of Chinese patent medicines demonstrates varied quality and lacks high-quality evidence, failing to meet the demands of policy-making, clinical decision-making, and industrial decision-making. To address this issue, this project gathered experts in clinical medicine, clinical pharmacy, evidence-based medicine, drug epidemiology, medical ethics, and policy and regulation in China. They referred to the model of international post-marketing research on medicines and developed Guidelines for post-marketing research on clinical effectiveness of Chinese patent medicines under the framework of relevant laws and regulations and technical guidance documents in China. The guidelines were developed with consideration to the characteristics of Chinese patent medicines, China's national conditions, and all the stakeholders including marketing authorization holders, clinical researchers, drug administration, and users. The development of the guidelines followed the requirements for developing group standards set by the China Association of Chinese Medicine. The guidelines fully implement the concept of full life-cycle research, emphasizing the combination of traditional Chinese medicine(TCM) theory, human use experience, and clinical trials and pay attention to the compliance, scientificity, and ethics of research. The guidelines clarify the topic selection and decision-making path of the post-marketing research on effectiveness of Chinese patent medicines through six

steps:

determining research purpose, analyzing drug characteristics, evaluating research basis, proposing clinical orientation, clarifying research purpose, and implementing classified research. The general principles of research design and implementation were clarified from eight aspects research type, research objects, sample size, efficacy indicators, bias, missing data, evidence level, and practicality. It focuses on the research on the TCM syndrome-based efficacy evaluation, clinical value-oriented mechanism of action, and the effectiveness of Chinese patent medicines with different routes of administration. The guidelines provide a universal methodological basis for the post-marketing research on clinical effectiveness of Chinese patent medicines.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Medicamentos de Ervas Chinesas / Medicamentos sem Prescrição Idioma: Zh Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Medicamentos de Ervas Chinesas / Medicamentos sem Prescrição Idioma: Zh Ano de publicação: 2024 Tipo de documento: Article