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Clinical Trial Summary

In this study, the therapeutic drug monitoring of teicoplanin is carried out among children to obtain the drug concentration, clinical efficacy and safety data of children patients in different gender and age groups. Then we analyze the relationship between blood drug concentration and efficacy and safety, and provide recommendations for the treatment window of teicoplanin in Chinese children.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03933748
Study type Observational
Source Shandong University
Contact Wei Zhao, Ph.D
Phone 86053188383308
Email zhao4wei2@hotmail.com
Status Recruiting
Phase
Start date April 1, 2019
Completion date December 2025

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