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Clinical Trial Summary

This is a multi-center, prospective, non-interventional cohort study .

Its primary objectives are:

1. assess DILI patients' clinical characteristics, disease progression and influencing factors in clinical practice;

2. learn about suspected drug caused DILI,rechallenging, liver biochemical abnormalities mode, etc.


Clinical Trial Description

The main purpose of this study is to understand patients with DILI clinical outcome and influencing factors in China's second and tertiary general hospitals (including Western medicine hospital, Chinese medicine hospital andIntegrated traditional Chinese and Western Medicine Hospital) and vulnerabilities of drug-induced liver injury specialist hospital (tuberculosis hospital, Pulmonary, etc.) in mainland.

The main purpose

1. assess the DILI patients' clinical outcomes and influencing factors in the real world;

2. learn about suspected drug caused DILI,rechallenging, liver biochemical abnormalities mode, etc.

Secondary objectives

1. assess the compliance of the DILI practice to the 2015 vision of the DILI guidelines in china.;

2. evaluate the histological features of DILI patients;

3. assessment DILI characteristics, prognosis and influencing factors in specific populations(such as the elderly, children with underlying liver disease background, etc.) ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02961413
Study type Observational
Source Drug Induced Liver Disease Study Group
Contact Chunxia Zhang
Email chunxia.zhang@unimedsci.com
Status Recruiting
Phase
Start date April 2016
Completion date December 2020

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