The necessity and feasibility of establishing technical specifications for registry of Chinese medicine clinical study.
- Author:
Peng-Fei LU
;
Xing LIAO
;
Yan-Ming XIE
;
Zhi-Guo WANG
- Publication Type:Journal Article
- MeSH:
Biomedical Research;
Humans;
Medicine, Chinese Traditional;
standards;
Registries
- From:
Chinese Journal of Integrated Traditional and Western Medicine
2015;35(1):14-18
- CountryChina
- Language:Chinese
-
Abstract:
International clinical trials register is one of the global measures to realize transparency in clinical trials and also one of a powerful measure to improve the quality of clinical trials. Many scholars studying the quality of TCM clinical trials find that they are poor in quality and lack transparency. Furthermore, they find that TCM clinical trial registry has many problems. We must base on the successful experiences of WHO and international clinical trial registry to establish technical specifications for registry of traditional Chinese medicine clinical study of their own. Then, it can effectively improve the overall level of TCM clinical studies. We have suggested some concrete and feasible measures to establish technical specifications for registry of traditional Chinese medicine clinical study of their own based on the problems of TCM clinical trial registry.
