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Clinical Trial Summary

This study is a retrospective, multi-center real world study. The real world data comes from the electronic medical record system and disease database of the research centers .The patient's demographic information, disease information, clinical treatment status, efficacy evaluation and adverse events and so on will be collected and evaluated by applicability of the data, generated an analysis data set. Use the causal inference method of statistical analysis to observe the effectiveness and safety of intravitreal injection of Conbercept, and explore the effectiveness and safety of different doses in the treatment of retinopathy of prematurity.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04985448
Study type Observational
Source Chengdu Kanghong Biotech Co., Ltd.
Contact
Status Enrolling by invitation
Phase
Start date September 2022
Completion date October 2022

See also
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