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Clinical Trial Summary

This trial is an exploratory study, aiming to explore the preliminary efficacy and safety of Kesuting Syrup in the treatment of novel coronavirus pneumonia. It is planned to include a total of 200 cases. Kesuting Syrup test group: Lianhua Qingwen Granules control group = 1:1, each 100 cases in each group.


Clinical Trial Description

This trial is a randomized, open-label, parallel-controlled clinical trial of active drugs.With reference to"Diagnosis and Treatment Protocol for COVID-19(Trial Version 9)", Lianhua Qingwen Granules have been recommended for mild and common patients during the medical observation period and clinical treatment period of the new coronavirus. The purpose of the experiment is preliminary evaluate the clinical efficacy and safety of Kesuting syrup in the treatment of COVID-19 (Light) . ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05366231
Study type Interventional
Source Guizhou Bailing Group Pharmaceutical Co Ltd
Contact
Status Completed
Phase Phase 4
Start date May 8, 2022
Completion date September 15, 2022

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