Bronchitis Clinical Trial
Official title:
A Multicenter, Randomized, Open Label, Add-on Study to Assess Efficacy and Safety of Xiyanping Injection in Subjects With Pediatric Bronchitis
This is a multicenter, randomized, open Label,add-on study.
This is an add-on study of efficacy and safety of intravenous injection of Xiyanping
injection in subjects with pediatric bronchitis.
The purpose to determine the efficacy and safety of conventional treatment combined with or
without Xiyanping injection in the treatment of pediatric bronchitis and to further evaluate
the clinical value of Xiyanping injection in shortening the course of pediatric bronchitis
The study will enroll 240 Pediatric bronchitis volunteers, who will be randomized into 2
groups (1:1 ratio): volunteers from the first group will receive Routine treatment for
pediatric bronchitis and Xiyanping injection; volunteers from the second group will receive
Routine treatment for pediatric bronchitis. Xiyanping injection will be administration as
intravenous injection of 0.2-0.4mL/kg/day once daily for 5 days concomitantly with Routine
treatment for pediatric bronchitis
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