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The Efficacy of Huaiqihuang Granule in Children With Primary Nephrotic Syndrome

Nephrotic Syndrome Clinical Trial

Official title:
A Real-world Study to Evaluate the Efficacy of Huaiqihuang Granule in Children With Primary Nephrotic Syndrome

Clinical Trial Summary

This is a multisite, open-label, prospective and registered study designed to evaluate the efficacy and safety of Huai-Qi-Huang granule in children with primary nephrotic syndrome.

Clinical Trial Description

This is a multisite, open-label, prospective and registered study designed to evaluate the efficacy and safety of Huai-Qi-Huang granule in children with primary nephrotic syndrome(PNS). The study will be Planned at 1500 participants, and subjects will be on study for up to one year. Data will be collected by authorized physicians for 48 weeks. all of the data included demographic characteristics, information about PNS, laboratory tests and adverse events. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03332420
Study type Observational
Source Qidong Gaitianli Medicines Co., Ltd
Contact
Status Completed
Phase
Start date November 16, 2017
Completion date August 31, 2021
View Details
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