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Clinical Trial Summary

Combined with the regional and population characteristics of Asia and Africa, Huashi Baidu Granule was used to intervene in mild and moderate patients with COVID-19, evaluate its efficacy and safety, and clarify its characteristics of action.


Clinical Trial Description

In this study, a double-blind, double dummy, randomized control method was used to include 300 cases of mild and moderate COVID-19 patients in three centers at home and abroad. The clinical efficacy of Huashi Baidu Granule and Monapiravir in intervening COVID-19 patients was compared, It is proved that Huashi Baidu Granule has the same clinical efficacy and safety against COVID-19 as Monapiravir, and its characteristics of action are clarified to obtain high-level clinical evidence-based medical evidence of Huashi Baidu Granule in treating COVID-19 mild and moderate. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05638672
Study type Interventional
Source Xiyuan Hospital of China Academy of Chinese Medical Sciences
Contact
Status Recruiting
Phase N/A
Start date May 6, 2023
Completion date June 1, 2024

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