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Post-marketing Safety Surveillance of Breviscapine Powder-Injection : a Registry Study

Adverse Drug Event Clinical Trial

Official title:
Post-marketing Safety Surveillance of Breviscapine Powder-Injection : a Registry Study

Clinical Trial Summary

This registry aims to monitor the safety of Breviscapine Powder-Injection and to identify the potential risk factors for the adverse drug reactions.

Clinical Trial Description

Breviscapine Powder-Injection is a kind of natural compound injection with high purity of Scutellarin-Na (over 98%). It's a popular drug for ischemic diseases, as cerebral ischemic stroke, coronary heart disease or angor pectoris. However, more and more case reports about the adverse drug events of Chinese medicine injections extracted from Dengzhanhua (herba erigernotis) (Breviscapine is one of the most common compounds in it) have been reported in recent 10 years. Therefore, this registry of Breviscapine Powder-Injection aims to monitor the safety of Breviscapine Powder-Injection and to identify the potential risk factors for the adverse drug reactions. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02559960
Study type Observational
Source China Academy of Chinese Medical Sciences
Contact
Status Suspended
Phase
Start date September 2015
Completion date December 2021
View Details
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