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Clinical Trial Summary

This study is a prospective, multicenter, randomized controlled trial and aims to evaluate efficacy and safety of Xuanfei Baidu Granule in the treatment of influenza A. This study plans to enroll 584 subjects. The subjects will be randomly divided into 4 groups according to the ratio of 1:1:1:1, and they will be treated with Xuanfei Baidu Granule Placebo, Xuanfei Baidu Granule, Xuanfei Baidu Granule combined with Baloxavir Marboxil tablet.1 bag of Xuanfei Baidu Granule and Xuanfei Baidu Granule Placebo in the morning and evening, and take with boiling water for 5 days. Baloxavir Marboxil Tablet was taken orally 2 tablets, once a day for 1 day. The subjects were visited every day for 7 days after enrollment.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06205641
Study type Interventional
Source Capital Medical University
Contact Zhaohui Tong, PhD
Phone 13910930309
Email tongzhaohuicy@sina.com
Status Recruiting
Phase N/A
Start date January 2024
Completion date January 2025

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